Prior to Clemson

11.  Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms

Metrano, A. J.; Chinn, A. J.; Shugrue, C. R.; Stone, E. A.; Kim, B.; Miller, S. J.

Chem. Rev. 2020, 120, 11479–11615.

nihms 1679793 f0001

10.  Application of High-Throughput Competition Experiments in the Development of Aspartate Directed Site-Selective Modification of Tyrosine Residues in Peptides

Chinn, A. J.; Hwang, J.; Kim, B.; Parish, C. A.; Krska, S. W.; Miller, S. J.

J. Org. Chem. 2020, 85, 9424–9433.

nihms 1679785 f0001

9.  A Stereodynamic Redox-Interconversion Network of Vicinal Tertiary and Quaternary Carbon Stereocenters in Hydroquinone-Quinone Hybrid Dihydrobenzofurans

Storch, G.; Kim, B.; Mercado, B. Q.; Miller, S. J.

Angew. Chem. Int. Ed. 201857, 15107–15111.

nihms 989994 f0003 1

8.  Hydrogenation Catalyst Generates Cyclic Peptide Stereocenters in Sequence

Le, D. N.; Hansen, E.; Khan, H. K.; Kim, B.; Wiest, O.; Dong, V. M.

Nat. Chem2018, 10, 968–973.

nihms 1026101 f0001 1

7.  Divergent Control of Point and Axial Stereogenicity: Catalytic Enantioselective C−N Bond- Forming Cross-Coupling and Catalyst-Controlled Atroposelective Cyclodehydration

Kwon, Y.; Chinn, A. J.; Kim, B.; Miller, S. J.

Angew. Chem. Int. Ed. 2018, 57, 6251–6255.


6.  Enantioselective Intermolecular C–O Bond Formation in the Desymmetrization of Diarylmethines Employing a Guanidinylated Peptide-Based Catalyst

Chinn, A. J.; Kim, B.; Kwon. Y.; Miller, S. J.

J. Am. Chem. Soc. 2017, 139, 18107–18114.


5.  Stereodynamic Quinone–Hydroquinone Molecules That Enantiomerize at sp3-Carbon via Redox-Interconversion

Kim, B.; Storch, G.; Banerjee, G.; Mercado, B. Q.; Castillo-Lora, J.; Brudvig, G. W.; Mayer, J. M.; Miller, S. J.

J. Am. Chem. Soc. 2017, 139, 15239–15244.


4.  Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullmann Cross-Coupling

Kim, B.; Chinn, A. J.; Fandrick, D. R.; Senanayake, C. H.; Singer, R. A.; Miller, S. J.

J. Am. Chem. Soc. 2016, 138, 7939–7945.

nihms 832004 f0001

3.  Inhibition of Steroid Sulfatase with 4-Substituted Estrone and Estradiol Derivatives

Phan, C.-M.; Liu, Y.; Kim, B.; Mostafa, Y.; Taylor, S. D.

Bioorg. Med. Chem. 2011, 19, 5999–6005.

2.  Phthalides by Rhodium-Catalyzed Ketone Hydroacylation

Phan, D. H. T.; Kim, B.; Dong, V. M.

J. Am. Soc. Chem. 2009, 131, 15608–15609.

1.  Synthesis of 4-Formyl Estrone Using a Positional Protecting Group and Its Conversion to Other C-4-Substituted Estrogens

Liu, Y.; Kim, B.; Taylor, S. D.

J. Org. Chem. 2007, 72, 8824–8830.


Clemson University
Department of Chemistry
Hunter Hall, 211 S. Palmetto Blvd
Clemson, SC 29634, USA


Lab – Hunter Hall 443, 446
Office – Hunter Hall 463

the kim group clemson paw and buldings