[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.27.6″ global_colors_info=”{}”][et_pb_row admin_label=”Class Details Area” _builder_version=”4.16″ custom_padding=”27px|0px|25px|0px||” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text admin_label=”Title” _builder_version=”4.27.6″ text_font=”||||||||” header_font=”Arial||||||||” header_2_font=”Arial|600|||||||” header_2_text_align=”center” header_2_font_size=”36px” header_2_line_height=”1.2em” custom_margin=”||0px|” custom_padding=”|||” animation_style=”fade” global_colors_info=”{}”]<\/p>\n
From Clemson<\/h2>\n
(\u2020 undergraduate student)<\/p>\n
<\/p>\n
[\/et_pb_text][et_pb_divider divider_position=”center” divider_weight=”3px” _builder_version=”4.17.0″ width_tablet=”” width_phone=”” width_last_edited=”on|desktop” max_width=”100px” max_width_tablet=”” max_width_phone=”” max_width_last_edited=”on|desktop” module_alignment=”center” animation_style=”slide” animation_direction=”top” animation_intensity_slide=”10%” animation_starting_opacity=”100%” global_colors_info=”{}”][\/et_pb_divider][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” custom_padding=”21px|||||” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”1.5em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
14. Enantioselective Deoxygenative Amino-Cyanation of Carboxylic Acids via Ti-Multicatalysis<\/strong><\/h3>\nGu tierrez, G.; Wilt, A. J.; Muhammad, S.; Girotti, E.\u2020; Rodriguez,D.\u2020; Kim, B.*<\/span><\/p>\n\n- Org. Lett.<\/em>\u00a02024<\/strong>, 26 (44)<\/em>, 9442\u20139447 <\/a><\/i><\/span><\/li>\n
- One of the Most Read Articles in Org. Lett. in Nov.<\/i><\/span><\/span><\/li>\n
- Highlighted in OPRD newsletter “Some Items of Interest to Process R&D Chemists and Engineers”<\/i><\/a><\/span><\/span><\/li>\n
- Highlighted in Synfacts<\/i> 2025; 21(01): 53.<\/a><\/i><\/i><\/i><\/span><\/i><\/span><\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2024\/10\/TOC.jpg” alt=”Graphic of Enantioselective Deoxygenative Amino-Cyanation of Carboxylic Acids via Ti-Multi-catalysis.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”100%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”1.5em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
13. Ammonium-Binding Bifunctional Aza-Crown Ether Catalysts for Substrate-Selective Hydroxyl Functionalization<\/strong><\/h3>\nSeilkop, A. G.; Odoh, A. S.; Coradi, N. J.\u2020; Wright, J. I.\u2020; Barroso, J.; Kim, B.*<\/h4>\n\n- J. Org. Chem. 2024, 89 (18), 13338\u201313344 <\/a><\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2024\/09\/TOC-pdf.jpg” alt=”Graphic of Ammonium-Binding Bifunctional Aza-Crown Ether Catalysts.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”100%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” custom_padding=”6px|||||” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
12.<\/strong><\/span> SuFEx-Enabled<\/strong> Direct Deoxy-Diversification of Alcohols<\/strong><\/span><\/h3>\n\n- Odoh, A. S.; <\/span>Keeler, C.\u2020; Kim, B.*<\/li>\n
- Org. Lett. 2024, 26 (18), <\/a>4013\u20134017<\/a><\/li>\n
- One of the Most Read Articles in Org. Lett. in May and June 2024.\u00a0<\/li>\n
- Highlighted in OPRD newsletter \u201cSome Items of Interest to Process R&D Chemists and Engineers\u201d<\/a><\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2024\/05\/OL-2024-TOC-copy.jpg” alt=”Graphic of Direct Deoxy-Diversification of Alcohols.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”100%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
11. Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms<\/strong><\/h3>\n\n- Metrano, A. J.; Chinn, A.J.; Shugrue, C. R.; Stone, E.A.; Kim, B.; Miller, S.J.<\/li>\n
- Chem. Rev. 2020, 120, 11479\u201311615.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms-1679793-f0001.jpeg” alt=”Graphic of Asymmetric Catalysis Mediated by Synthetic Peptides.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”70%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
10. Application of High-Throughput Competition Experiments in the Development of Aspartate Directed Site-Selective Modification of Tyrosine Residues in Peptides<\/strong><\/h3>\n\n- Chinn, A.J.; Hwang, J.; Kim, B.; Parish, C. A.; Krska, S. W.; Miller, S.J.<\/li>\n
- J. Org. Chem. 2020, 85, 9424\u20139433.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms-1679785-f0001.jpeg” alt=”Graphic of Aspartate Directed Site-Selective Modification of Tyrosine Residues in Peptides.” _builder_version=”4.27.6″ _module_preset=”default” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row admin_label=”Class Details Area” _builder_version=”4.16″ custom_padding=”27px|0px|60px|0px” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text admin_label=”Title” _builder_version=”4.17.0″ text_font=”||||||||” header_font=”Arial||||||||” header_2_font=”Arial|600|||||||” header_2_text_align=”center” header_2_font_size=”36px” header_2_line_height=”1.2em” custom_margin=”||0px|” custom_padding=”|||” animation_style=”fade” global_colors_info=”{}”]<\/p>\n
Mentored Work<\/h2>\n
[\/et_pb_text][et_pb_divider divider_position=”center” divider_weight=”3px” _builder_version=”4.17.0″ width_tablet=”” width_phone=”” width_last_edited=”on|desktop” max_width=”100px” max_width_tablet=”” max_width_phone=”” max_width_last_edited=”on|desktop” module_alignment=”center” animation_style=”slide” animation_direction=”top” animation_intensity_slide=”10%” animation_starting_opacity=”100%” global_colors_info=”{}”][\/et_pb_divider][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
9. A Stereodynamic Redox-Interconversion Network of Vicinal Tertiary and Quaternary Carbon Stereocenters in Hydroquinone-Quinone Hybrid Dihydrobenzofurans<\/strong><\/h3>\n\n- Storch, G.; Kim, B.; Mercado, B. Q.; Miller, S.J.<\/li>\n
- Angew. Chem. Int. Ed.\u00a02018,\u00a057, 15107\u201315111.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/nihms-989994-f0003-1.jpg” alt=”Graphic of Vicinal Tertiary and Quaternary Carbon Stereocenters.” _builder_version=”4.27.6″ _module_preset=”default” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
8. Hydrogenation Catalyst Generates Cyclic Peptide Stereocenters in Sequence<\/strong><\/h3>\n\n- Le, D.N.; Hansen, E.; Khan, H.K.; Kim, B.; Wiest, O.; Dong, V.M.<\/li>\n
- Nat. Chem.\u00a02018, 10, 968\u2013973.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/nihms-1026101-f0001-1.jpg” alt=”Graphic of Hydrogenation Catalyst Generates Cyclic Peptide Stereocenters in Sequence.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
7. Divergent Control of Point and Axial Stereogenicity: Catalytic Enantioselective C\u2212N Bond- Forming Cross-Coupling and Catalyst-Controlled Atroposelective Cyclodehydration<\/strong><\/h3>\n\n- Kwon, Y.; Chinn, A.J.; Kim, B.; Miller, S.J.<\/li>\n
- Angew. Chem. Int. Ed. 2018, 57, 6251\u20136255.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms965698u1.jpeg” alt=”Graphic of Divergent Control of Point and Axial Stereogenicity.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
6. Enantioselective Intermolecular C\u2013O Bond Formation in the Desymmetrization of Diarylmethines Employing a Guanidinylated Peptide-Based Catalyst<\/strong><\/h3>\n\n- Chinn, A.J.; Kim, B.; Kwon. Y.; Miller, S.J.<\/li>\n
- J. Am. Chem. Soc. 2017, 139, 18107\u201318114.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms926561u1.jpeg” alt=”Graphic of Enantioselective Intermolecular C\u2013O Bond Formation.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
5. Stereodynamic Quinone-Hydroquinone Molecules That Enantiomerize at sp3-Carbon via Redox-Interconversion<\/strong><\/h3>\n\n- Kim, B.; Storch, G.; Banerjee, G.; Mercado, B.Q.; Castillo-Lora, J.; Brudvig, G. W.; Mayer, J.M.; Miller, S.J.<\/li>\n
- J. Am. Chem. Soc. 2017, 139, 15239\u201315244.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms926557u1.jpeg” alt=”Graphic of Stereodynamic Quinone-Hydroquinone Molecules.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
4. Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullmann Cross-Coupling<\/strong><\/h3>\n\n- Kim, B.; Chinn, A. J.; Fandrick, D. R.; Senanayake, C. H.; Singer, R. A.; Miller, S. J.<\/li>\n
- J. Am. Chem. Soc. 2016, 138, 7939\u20137945.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms-832004-f0001.jpeg” alt=”Graphic of Distal Stereocontrol Using Guanidinylated Peptides.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
3. Inhibition of Steroid Sulfatase with 4-Substituted Estrone and Estradiol Derivatives<\/strong><\/h3>\n\n- Phan, C.M.; Liu, Y.; Kim, B.; Mostafa, Y.; Taylor, S.D.<\/li>\n
- Bioorg. Med. Chem. 2011, 19, 5999\u20136005.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/1-s2.0-S0968089611006808-fx1-1.jpg” alt=”Graphic of Inhibition of Steroid Sulfatase.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
2. Phthalides by Rhodium-Catalyzed Ketone Hydroacylation<\/strong><\/h3>\n\n- Phan, D.H.T.; Kim, B.; Dong, V.M.<\/li>\n
- J. Am. Soc. Chem. 2009, 131, 15608\u201315609.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/ja-2009-07711a_0004.gif” alt=”Graphic of Phthalides by Rhodium-Catalyzed Ketone Hydroacylation.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
1. Synthesis of 4-Formyl Estrone Using a Positional Protecting Group and Its Conversion to Other C-4-Substituted Estrogens<\/strong><\/h3>\n\n- Liu, Y.; Kim, B.; Taylor, S.D.<\/li>\n
- J. Org. Chem. 2007, 72, 8824\u20138830.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/jo7017075n00001.gif” alt=”Graphic of Synthesis of 4-Formyl Estrone.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Divider Section” _builder_version=”4.16″ background_color=”rgba(0,0,0,0.93)” custom_padding=”0px||0px|” global_colors_info=”{}”][et_pb_row admin_label=”Divider Area” _builder_version=”4.16″ custom_padding=”0px||0px|” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_divider show_divider=”off” _builder_version=”4.16″ global_colors_info=”{}”][\/et_pb_divider][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Footer Section” _builder_version=”3.23.3″ background_color=”rgba(0,0,0,0.93)” custom_padding=”90px||90px|” global_module=”128″ saved_tabs=”all” global_colors_info=”{}”][et_pb_row column_structure=”1_3,1_3,1_3″ admin_label=”Footer Area” _builder_version=”4.16″ global_colors_info=”{}”][et_pb_column type=”1_3″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text ul_type=”none” admin_label=”Title” _builder_version=”4.16″ text_font=”Arial||||||||” text_text_color=”rgba(255,255,255,0.7)” text_font_size=”16px” text_line_height=”1.8em” ul_font=”Poppins||||||||” ul_text_align=”center” header_font=”||||||||” header_2_font=”Poppins||||||||” header_2_text_align=”center” header_2_font_size=”24px” header_2_line_height=”1.4em” text_orientation=”center” background_layout=”dark” custom_margin=”||15px|” custom_padding=”|||” animation_style=”fade” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
Address<\/span><\/strong><\/h2>\nClemson University
Department of Chemistry
Hunter Hall, 211 S. Palmetto Blvd
Clemson, SC 29634, USA<\/p>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text ul_type=”none” admin_label=”Title” _builder_version=”4.27.6″ text_font=”Poppins||||||||” text_text_color=”rgba(255,255,255,0.7)” text_font_size=”16px” text_line_height=”1.8em” ul_font=”Poppins||||||||” ul_text_align=”center” header_font=”||||||||” header_2_font=”Poppins||||||||” header_2_text_align=”center” header_2_font_size=”24px” header_2_line_height=”1.4em” text_orientation=”center” background_layout=”dark” custom_margin=”||15px|” custom_padding=”|||” animation_style=”fade” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
Contact<\/span><\/strong><\/h2>\n
- \n
- Org. Lett.<\/em>\u00a02024<\/strong>, 26 (44)<\/em>, 9442\u20139447 <\/a><\/i><\/span><\/li>\n
- One of the Most Read Articles in Org. Lett. in Nov.<\/i><\/span><\/span><\/li>\n
- Highlighted in OPRD newsletter “Some Items of Interest to Process R&D Chemists and Engineers”<\/i><\/a><\/span><\/span><\/li>\n
- Highlighted in Synfacts<\/i> 2025; 21(01): 53.<\/a><\/i><\/i><\/i><\/span><\/i><\/span><\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2024\/10\/TOC.jpg” alt=”Graphic of Enantioselective Deoxygenative Amino-Cyanation of Carboxylic Acids via Ti-Multi-catalysis.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”100%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”1.5em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
13. Ammonium-Binding Bifunctional Aza-Crown Ether Catalysts for Substrate-Selective Hydroxyl Functionalization<\/strong><\/h3>\n
Seilkop, A. G.; Odoh, A. S.; Coradi, N. J.\u2020; Wright, J. I.\u2020; Barroso, J.; Kim, B.*<\/h4>\n
- \n
- J. Org. Chem. 2024, 89 (18), 13338\u201313344 <\/a><\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2024\/09\/TOC-pdf.jpg” alt=”Graphic of Ammonium-Binding Bifunctional Aza-Crown Ether Catalysts.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”100%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” custom_padding=”6px|||||” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
12.<\/strong><\/span> SuFEx-Enabled<\/strong> Direct Deoxy-Diversification of Alcohols<\/strong><\/span><\/h3>\n
- \n
- Odoh, A. S.; <\/span>Keeler, C.\u2020; Kim, B.*<\/li>\n
- Org. Lett. 2024, 26 (18), <\/a>4013\u20134017<\/a><\/li>\n
- One of the Most Read Articles in Org. Lett. in May and June 2024.\u00a0<\/li>\n
- Highlighted in OPRD newsletter \u201cSome Items of Interest to Process R&D Chemists and Engineers\u201d<\/a><\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2024\/05\/OL-2024-TOC-copy.jpg” alt=”Graphic of Direct Deoxy-Diversification of Alcohols.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”100%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
11. Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms<\/strong><\/h3>\n
- \n
- Metrano, A. J.; Chinn, A.J.; Shugrue, C. R.; Stone, E.A.; Kim, B.; Miller, S.J.<\/li>\n
- Chem. Rev. 2020, 120, 11479\u201311615.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms-1679793-f0001.jpeg” alt=”Graphic of Asymmetric Catalysis Mediated by Synthetic Peptides.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”70%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
10. Application of High-Throughput Competition Experiments in the Development of Aspartate Directed Site-Selective Modification of Tyrosine Residues in Peptides<\/strong><\/h3>\n
- \n
- Chinn, A.J.; Hwang, J.; Kim, B.; Parish, C. A.; Krska, S. W.; Miller, S.J.<\/li>\n
- J. Org. Chem. 2020, 85, 9424\u20139433.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms-1679785-f0001.jpeg” alt=”Graphic of Aspartate Directed Site-Selective Modification of Tyrosine Residues in Peptides.” _builder_version=”4.27.6″ _module_preset=”default” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row admin_label=”Class Details Area” _builder_version=”4.16″ custom_padding=”27px|0px|60px|0px” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text admin_label=”Title” _builder_version=”4.17.0″ text_font=”||||||||” header_font=”Arial||||||||” header_2_font=”Arial|600|||||||” header_2_text_align=”center” header_2_font_size=”36px” header_2_line_height=”1.2em” custom_margin=”||0px|” custom_padding=”|||” animation_style=”fade” global_colors_info=”{}”]<\/p>\n
Mentored Work<\/h2>\n
[\/et_pb_text][et_pb_divider divider_position=”center” divider_weight=”3px” _builder_version=”4.17.0″ width_tablet=”” width_phone=”” width_last_edited=”on|desktop” max_width=”100px” max_width_tablet=”” max_width_phone=”” max_width_last_edited=”on|desktop” module_alignment=”center” animation_style=”slide” animation_direction=”top” animation_intensity_slide=”10%” animation_starting_opacity=”100%” global_colors_info=”{}”][\/et_pb_divider][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” min_height=”107px” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” text_line_height=”3em” header_4_font=”Arial||||||||” header_4_font_size=”16px” text_line_height_tablet=”3em” text_line_height_phone=”3em” text_line_height_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
9. A Stereodynamic Redox-Interconversion Network of Vicinal Tertiary and Quaternary Carbon Stereocenters in Hydroquinone-Quinone Hybrid Dihydrobenzofurans<\/strong><\/h3>\n
- \n
- Storch, G.; Kim, B.; Mercado, B. Q.; Miller, S.J.<\/li>\n
- Angew. Chem. Int. Ed.\u00a02018,\u00a057, 15107\u201315111.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/nihms-989994-f0003-1.jpg” alt=”Graphic of Vicinal Tertiary and Quaternary Carbon Stereocenters.” _builder_version=”4.27.6″ _module_preset=”default” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
8. Hydrogenation Catalyst Generates Cyclic Peptide Stereocenters in Sequence<\/strong><\/h3>\n
- \n
- Le, D.N.; Hansen, E.; Khan, H.K.; Kim, B.; Wiest, O.; Dong, V.M.<\/li>\n
- Nat. Chem.\u00a02018, 10, 968\u2013973.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/nihms-1026101-f0001-1.jpg” alt=”Graphic of Hydrogenation Catalyst Generates Cyclic Peptide Stereocenters in Sequence.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
7. Divergent Control of Point and Axial Stereogenicity: Catalytic Enantioselective C\u2212N Bond- Forming Cross-Coupling and Catalyst-Controlled Atroposelective Cyclodehydration<\/strong><\/h3>\n
- \n
- Kwon, Y.; Chinn, A.J.; Kim, B.; Miller, S.J.<\/li>\n
- Angew. Chem. Int. Ed. 2018, 57, 6251\u20136255.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms965698u1.jpeg” alt=”Graphic of Divergent Control of Point and Axial Stereogenicity.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
6. Enantioselective Intermolecular C\u2013O Bond Formation in the Desymmetrization of Diarylmethines Employing a Guanidinylated Peptide-Based Catalyst<\/strong><\/h3>\n
- \n
- Chinn, A.J.; Kim, B.; Kwon. Y.; Miller, S.J.<\/li>\n
- J. Am. Chem. Soc. 2017, 139, 18107\u201318114.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms926561u1.jpeg” alt=”Graphic of Enantioselective Intermolecular C\u2013O Bond Formation.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
5. Stereodynamic Quinone-Hydroquinone Molecules That Enantiomerize at sp3-Carbon via Redox-Interconversion<\/strong><\/h3>\n
- \n
- Kim, B.; Storch, G.; Banerjee, G.; Mercado, B.Q.; Castillo-Lora, J.; Brudvig, G. W.; Mayer, J.M.; Miller, S.J.<\/li>\n
- J. Am. Chem. Soc. 2017, 139, 15239\u201315244.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms926557u1.jpeg” alt=”Graphic of Stereodynamic Quinone-Hydroquinone Molecules.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
4. Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullmann Cross-Coupling<\/strong><\/h3>\n
- \n
- Kim, B.; Chinn, A. J.; Fandrick, D. R.; Senanayake, C. H.; Singer, R. A.; Miller, S. J.<\/li>\n
- J. Am. Chem. Soc. 2016, 138, 7939\u20137945.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2022\/08\/nihms-832004-f0001.jpeg” alt=”Graphic of Distal Stereocontrol Using Guanidinylated Peptides.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
3. Inhibition of Steroid Sulfatase with 4-Substituted Estrone and Estradiol Derivatives<\/strong><\/h3>\n
- \n
- Phan, C.M.; Liu, Y.; Kim, B.; Mostafa, Y.; Taylor, S.D.<\/li>\n
- Bioorg. Med. Chem. 2011, 19, 5999\u20136005.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/1-s2.0-S0968089611006808-fx1-1.jpg” alt=”Graphic of Inhibition of Steroid Sulfatase.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
2. Phthalides by Rhodium-Catalyzed Ketone Hydroacylation<\/strong><\/h3>\n
- \n
- Phan, D.H.T.; Kim, B.; Dong, V.M.<\/li>\n
- J. Am. Soc. Chem. 2009, 131, 15608\u201315609.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/ja-2009-07711a_0004.gif” alt=”Graphic of Phthalides by Rhodium-Catalyzed Ketone Hydroacylation.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_2,1_2″ _builder_version=”4.17.0″ width=”90%” locked=”off” global_colors_info=”{}”][et_pb_column type=”1_2″ _builder_version=”4.17.0″ _module_preset=”default” custom_padding=”||0px||false|false” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.6″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n
1. Synthesis of 4-Formyl Estrone Using a Positional Protecting Group and Its Conversion to Other C-4-Substituted Estrogens<\/strong><\/h3>\n
- \n
- Liu, Y.; Kim, B.; Taylor, S.D.<\/li>\n
- J. Org. Chem. 2007, 72, 8824\u20138830.<\/li>\n<\/ul>\n
[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.17.0″ custom_padding=”||0px||false|false” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/04\/jo7017075n00001.gif” alt=”Graphic of Synthesis of 4-Formyl Estrone.” align=”center” _builder_version=”4.27.6″ _module_preset=”default” width=”80%” box_shadow_style=”preset1″ global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Divider Section” _builder_version=”4.16″ background_color=”rgba(0,0,0,0.93)” custom_padding=”0px||0px|” global_colors_info=”{}”][et_pb_row admin_label=”Divider Area” _builder_version=”4.16″ custom_padding=”0px||0px|” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_divider show_divider=”off” _builder_version=”4.16″ global_colors_info=”{}”][\/et_pb_divider][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Footer Section” _builder_version=”3.23.3″ background_color=”rgba(0,0,0,0.93)” custom_padding=”90px||90px|” global_module=”128″ saved_tabs=”all” global_colors_info=”{}”][et_pb_row column_structure=”1_3,1_3,1_3″ admin_label=”Footer Area” _builder_version=”4.16″ global_colors_info=”{}”][et_pb_column type=”1_3″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text ul_type=”none” admin_label=”Title” _builder_version=”4.16″ text_font=”Arial||||||||” text_text_color=”rgba(255,255,255,0.7)” text_font_size=”16px” text_line_height=”1.8em” ul_font=”Poppins||||||||” ul_text_align=”center” header_font=”||||||||” header_2_font=”Poppins||||||||” header_2_text_align=”center” header_2_font_size=”24px” header_2_line_height=”1.4em” text_orientation=”center” background_layout=”dark” custom_margin=”||15px|” custom_padding=”|||” animation_style=”fade” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
Address<\/span><\/strong><\/h2>\n
Clemson University
Department of Chemistry
Hunter Hall, 211 S. Palmetto Blvd
Clemson, SC 29634, USA<\/p>\n[\/et_pb_text][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text ul_type=”none” admin_label=”Title” _builder_version=”4.27.6″ text_font=”Poppins||||||||” text_text_color=”rgba(255,255,255,0.7)” text_font_size=”16px” text_line_height=”1.8em” ul_font=”Poppins||||||||” ul_text_align=”center” header_font=”||||||||” header_2_font=”Poppins||||||||” header_2_text_align=”center” header_2_font_size=”24px” header_2_line_height=”1.4em” text_orientation=”center” background_layout=”dark” custom_margin=”||15px|” custom_padding=”|||” animation_style=”fade” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n
Contact<\/span><\/strong><\/h2>\n
- Org. Lett. 2024, 26 (18), <\/a>4013\u20134017<\/a><\/li>\n
- Odoh, A. S.; <\/span>Keeler, C.\u2020; Kim, B.*<\/li>\n
- One of the Most Read Articles in Org. Lett. in Nov.<\/i><\/span><\/span><\/li>\n
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\u00a0<\/p>\n