{"id":83,"date":"2020-03-03T16:04:58","date_gmt":"2020-03-03T16:04:58","guid":{"rendered":"https:\/\/scienceweb.clemson.edu\/boni\/?page_id=83"},"modified":"2025-10-03T02:38:07","modified_gmt":"2025-10-03T02:38:07","slug":"publications","status":"publish","type":"page","link":"https:\/\/scienceweb.clemson.edu\/kimgroup\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"

[et_pb_section fb_built=”1″ admin_label=”Page Title Section” _builder_version=”4.27.4″ background_image=”https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-content\/uploads\/sites\/6\/2020\/03\/10.jpg” background_blend=”multiply” height=”335px” height_tablet=”335px” height_phone=”335px” height_last_edited=”on|desktop” custom_padding=”110px||110px|” global_colors_info=”{}”][et_pb_row admin_label=”Page Title Area” _builder_version=”4.16″ background_size=”initial” background_position=”top_left” background_repeat=”repeat” 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=”4.16″ text_font=”||||||||” header_font=”Arial|700||||on|||” header_font_size=”60px” header_letter_spacing=”3px” header_2_font=”||||||||” header_2_font_size=”60px” background_layout=”dark” custom_margin=”||20px|” custom_padding=”|||” animation_style=”fade” header_font_size_tablet=”” header_font_size_phone=”40px” header_font_size_last_edited=”on|phone” inline_fonts=”Arial” global_colors_info=”{}”]<\/p>\n

Publications<\/span><\/h1>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.16″ 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=”4.27.4″ 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

(\u2020undergraduate student)<\/h3>\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=”4.27.4″ _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

14. Enantioselective Deoxygenative Amino-Cyanation of Carboxylic Acids via Ti-Multicatalysis<\/strong><\/span><\/h4>\n

Gutierrez, G.; Wilt, A. J.; Muhammad, S.; Girotti, E.\u2020; Rodriguez, D.\u2020; Kim, B.*<\/span><\/h4>\n

Org. Lett.<\/em>\u00a02024<\/strong>, 26 (44)<\/em>, 9442\u20139447 <\/a><\/i><\/span><\/h4>\n

\u2022\u00a0 <\/i>One of the Most Read Articles in Org. Lett. in Nov.<\/i><\/span><\/span><\/h4>\n

\u2022\u00a0 <\/i>Highlighted in OPRD newsletter “Some Items of Interest to Process R&D Chemists and Engineers”<\/i><\/a><\/span><\/span><\/h4>\n

\u2022\u00a0 <\/i>Highlighted in Synfacts<\/i> 2025; 21(01): 53.<\/a><\/i><\/i><\/i><\/span><\/i><\/span><\/h4>\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=”TOC” title_text=”TOC” align=”center” _builder_version=”4.27.0″ _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=”4.27.4″ _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

13. Ammonium-Binding Bifunctional Aza-Crown Ether Catalysts for Substrate-Selective Hydroxyl Functionalization<\/strong><\/span><\/h4>\n

Seilkop, A. G.; Odoh, A. S.; Coradi, N. J.\u2020; Wright, J. I.\u2020; Barroso, J.; Kim, B.*<\/span><\/h4>\n

J. Org. Chem.<\/em> 2024<\/strong>, 89 (18)<\/em>, 13338\u201313344 <\/a><\/i><\/span><\/h4>\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=”OL 2024 TOC copy” title_text=”TOC” align=”center” _builder_version=”4.20.2″ _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=”4.27.4″ _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

12. SuFEx-Enabled Direct Deoxy-Diversification of Alcohols<\/strong><\/span><\/h4>\n

Odoh, A. S.; Keeler, C.\u2020; Kim, B.*<\/span><\/h4>\n

Org. Lett.<\/em> 2024<\/strong>, 26 (18)<\/em>, <\/a>4013\u20134017<\/a>
<\/i><\/span><\/h4>\n

\u2022\u00a0 One of the Most Read Articles in Org. Lett. in May and June 2024.\u00a0<\/i><\/span><\/span><\/h4>\n

\u2022\u00a0 <\/i>Highlighted in OPRD newsletter “Some Items of Interest to Process R&D Chemists and Engineers”<\/i><\/a><\/span><\/h4>\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=”OL 2024 TOC copy” title_text=”OL 2024 TOC copy” align=”center” _builder_version=”4.20.2″ _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=”4.27.4″ _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.\u00a0 Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms<\/strong><\/span><\/h4>\n

Metrano, A. J.; Chinn, A. J.; Shugrue, C. R.; Stone, E. A.; Kim, B.; Miller, S. J.<\/span><\/h4>\n

Chem. Rev.<\/em> 2020<\/strong>, 120<\/em>, 11479\u201311615.<\/span><\/h4>\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=”nihms 1679793 f0001″ title_text=”nihms 1679793 f0001″ align=”center” _builder_version=”4.17.0″ _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=”4.27.4″ _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.\u00a0 Application of High-Throughput Competition Experiments in the Development of Aspartate Directed Site-Selective Modification of Tyrosine Residues in Peptides<\/strong><\/span><\/h4>\n

Chinn, A. J.; Hwang, J.; Kim, B.; Parish, C. A.; Krska, S. W.; Miller, S. J.<\/span><\/h4>\n

J. Org. Chem.<\/em> 2020<\/strong>, 85<\/em>, 9424\u20139433.<\/span><\/h4>\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=”nihms 1679785 f0001″ title_text=”nihms 1679785 f0001″ _builder_version=”4.17.0″ _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=”4.27.4″ _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.\u00a0 A Stereodynamic Redox-Interconversion Network of Vicinal Tertiary and Quaternary Carbon Stereocenters in Hydroquinone-Quinone Hybrid Dihydrobenzofurans<\/strong><\/span><\/h4>\n

Storch, G.; Kim, B.; Mercado, B. Q.; Miller, S. J.<\/span><\/h4>\n

Angew. Chem. Int. Ed.<\/em>\u00a02018<\/strong>,\u00a057<\/em>, 15107\u201315111.<\/span><\/h4>\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=”nihms 989994 f0003 1″ title_text=”nihms 989994 f0003 1″ _builder_version=”4.17.0″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

8.\u00a0 <\/strong>Hydrogenation Catalyst Generates Cyclic Peptide Stereocenters in Sequence<\/b><\/span><\/h4>\n

Le, D. N.; Hansen, E.; Khan, H. K.;\u00a0Kim, B.; Wiest, O.; Dong, V. M.<\/span><\/h4>\n

Nat. Chem<\/em>.\u00a02018<\/b>, 10<\/em>, 968\u2013973.<\/span><\/h4>\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=”nihms 1026101 f0001 1″ title_text=”nihms 1026101 f0001 1″ align=”center” _builder_version=”4.17.0″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

7.\u00a0 <\/strong>Divergent Control of Point and Axial Stereogenicity: Catalytic Enantioselective C\u2212N Bond- Forming Cross-Coupling and Catalyst-Controlled Atroposelective Cyclodehydration<\/b><\/span><\/h4>\n

Kwon, Y.; Chinn, A. J.; Kim, B.; Miller, S. J.<\/span><\/h4>\n

Angew. Chem. Int. Ed.<\/em> 2018<\/strong>, 57<\/em>, 6251\u20136255.<\/span><\/h4>\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=”nihms965698u1″ title_text=”nihms965698u1″ align=”center” _builder_version=”4.17.0″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

6.\u00a0 <\/strong>Enantioselective Intermolecular C\u2013O Bond Formation in the Desymmetrization of Diarylmethines Employing a Guanidinylated Peptide-Based Catalyst<\/b><\/span><\/h4>\n

Chinn, A. J.; Kim, B.; Kwon. Y.; Miller, S. J.<\/span><\/h4>\n

J. Am. Chem. Soc.<\/em> 2017<\/strong>, 139<\/em>, 18107\u201318114.<\/span><\/h4>\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=”nihms926561u1″ title_text=”nihms926561u1″ align=”center” _builder_version=”4.17.0″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

5.\u00a0 <\/strong>Stereodynamic Quinone\u2013Hydroquinone Molecules That Enantiomerize at sp3-Carbon via Redox-Interconversion<\/b><\/span><\/h4>\n

Kim, B.; Storch, G.; Banerjee, G.; Mercado, B. Q.; Castillo-Lora, J.; Brudvig, G. W.; Mayer, J. M.; Miller, S. J.<\/span><\/h4>\n

J. Am. Chem. Soc.<\/em> 2017<\/strong>, 139<\/em>, 15239\u201315244.<\/span><\/h4>\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=”nihms926557u1″ title_text=”nihms926557u1″ align=”center” _builder_version=”4.17.0″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

4.\u00a0 <\/strong>Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullmann Cross-Coupling<\/b><\/span><\/h4>\n

Kim, B.; Chinn, A. J.; Fandrick, D. R.; Senanayake, C. H.; Singer, R. A.; Miller, S. J.<\/span><\/h4>\n

J. Am. Chem. Soc.<\/em> 2016<\/strong>, 138<\/em>, 7939\u20137945.<\/span><\/h4>\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=”nihms 832004 f0001″ title_text=”nihms 832004 f0001″ align=”center” _builder_version=”4.17.0″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

3.\u00a0 <\/strong>Inhibition of Steroid Sulfatase with 4-Substituted Estrone and Estradiol Derivatives<\/b><\/span><\/h4>\n

Phan, C.-M.; Liu, Y.; Kim, B.; Mostafa, Y.; Taylor, S. D.<\/span><\/h4>\n

Bioorg. Med. Chem.<\/em> 2011<\/strong>, 19<\/em>, 5999\u20136005.<\/span><\/h4>\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=”1 s2.0 S0968089611006808 fx1 1″ title_text=”1 s2.0 S0968089611006808 fx1 1″ align=”center” _builder_version=”4.20.2″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

2.\u00a0 <\/strong>Phthalides by Rhodium-Catalyzed Ketone Hydroacylation<\/b><\/span><\/h4>\n

Phan, D. H. T.; Kim, B.; Dong, V. M.<\/span><\/h4>\n

J. Am. Soc. Chem.<\/em> 2009<\/strong>, 131<\/em>, 15608\u201315609.<\/span><\/h4>\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=”ja 2009 07711a 0004″ title_text=”ja 2009 07711a 0004″ align=”center” _builder_version=”4.20.2″ _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=”4.27.4″ _module_preset=”default” text_font=”Arial||||||||” text_font_size=”16px” header_font=”Arial||||||||” header_4_font_size=”16px” global_colors_info=”{}”]<\/p>\n

1.\u00a0 <\/strong>Synthesis of 4-Formyl Estrone Using a Positional Protecting Group and Its Conversion to Other C-4-Substituted Estrogens<\/b><\/span><\/h4>\n

Liu, Y.; Kim, B.; Taylor, S. D.<\/span><\/h4>\n

J. Org. Chem. <\/em>2007<\/strong>, 72<\/em>, 8824\u20138830.<\/span><\/h4>\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=”jo7017075n00001″ title_text=”jo7017075n00001″ align=”center” _builder_version=”4.20.2″ _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

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Contact<\/span><\/strong><\/h2>\n

Lab \u2013 Hunter Hall 443, 446
Office \u2013 Hunter Hall 463
byoungk@clemson.edu<\/a>
<\/span>864-656-1666<\/span><\/p>\n

<\/span><\/p>\n

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\"the\u00a0<\/p>\n

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Learn more about the Clemson University College of Science<\/a><\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"

PublicationsFrom Clemson (\u2020undergraduate student)  14. Enantioselective Deoxygenative Amino-Cyanation of Carboxylic Acids via Ti-Multicatalysis Gutierrez, G.; Wilt, A. J.; Muhammad, S.; Girotti, E.\u2020; Rodriguez, D.\u2020; Kim, B.* Org. Lett.\u00a02024, 26 (44), 9442\u20139447 \u2022\u00a0 One of the Most Read Articles in Org. Lett. in Nov. \u2022\u00a0 Highlighted in OPRD newsletter “Some Items of Interest to Process R&D […]<\/p>\n","protected":false},"author":4,"featured_media":0,"parent":0,"menu_order":9,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"class_list":["post-83","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-json\/wp\/v2\/pages\/83","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-json\/wp\/v2\/comments?post=83"}],"version-history":[{"count":0,"href":"https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-json\/wp\/v2\/pages\/83\/revisions"}],"wp:attachment":[{"href":"https:\/\/scienceweb.clemson.edu\/kimgroup\/wp-json\/wp\/v2\/media?parent=83"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}