Chang‐Sun Lee

发表

β-Methanesulfonyl-L-valine as a novel, unnatural amino acid surrogate for P2 in the design of HIV protease inhibitors.

Y. Kwon, Ho-il Choi, J. Koh, 1996 .

Novel, potent, selective, and orally bioavailable human betaII-tryptase inhibitors.

M. Mcgrath, Rohan V Mendonca, J. Janc, 2006, Bioorganic & medicinal chemistry letters.

Design of novel, potent, and selective human β-tryptase inhibitors based on α-keto-[1,2,4]-oxadiazoles

J. R. Somoza, M. Mcgrath, J. Janc, 2006 .

Structure-guided design of peptide-based tryptase inhibitors.

Yang Liu, James W Janc, J. R. Somoza, 2006, Biochemistry.

Total synthesis of (+)-kalkitoxin.

James D White, Chang‐Sun Lee, Qing-Chun Xu, 2003, Chemical Communications.

DESIGN, SYNTHESIS, AND CHARACTERIZATION OF DIPEPTIDE ISOSTERE CONTAINING CIS-EPOXIDE FOR THE IRREVERSIBLE INACTIVATION OF HIV PROTEASE

Sangsoo Kim, J. Ok, Ho-il Choi, 1996 .

Rational design of irreversible, pseudo-C2-symmetric hiv-1 protease inhibitors

Ho-il Choi, K. Moon, J. Koh, 1995 .

Total synthesis and biological evaluation of +-kalkitoxin, a cytotoxic metabolite of the cyanobacterium Lyngbya majuscula.

F. Valeriote, James D White, Chang‐Sun Lee, 2004, Organic & biomolecular chemistry.

Constrained analogs of methionine: asymmetric synthesis of χ-angle restricted methionine derivatives through [3.1.0]-γ-lactone cyclopropane ring opening

A. Hamilton, Kee-In Lee, Chang‐Sun Lee, 2001 .

Constrained Analogues of Methionine: Asymmetric Synthesis of χ-Angle Restricted Methionine Derivatives Through [3.1.0]-γ-Lactone Cyclopropane Ring Opening.

A. Hamilton, Kee-In Lee, Chang‐Sun Lee, 2001 .

(R)‐(+)‐3,4‐Dimethylcyclohex‐2‐en‐1‐one

James D White, U. Grether, Chang‐Sun Lee, 2005 .