Sang Wong Kim

发表

Identification of a quinoxaline derivative that is a potent telomerase inhibitor leading to cellular senescence of human cancer cells.

I. Chung, Joo Hee Kim, Joo Hee Kim, 2003, The Biochemical journal.

Quinazolines as potent and highly selective PDE5 inhibitors as potential therapeutics for male erectile dysfunction.

S. Ahn, Young Hoon Kim, N. Choi, 2008, Bioorganic & medicinal chemistry letters.

Access to cis-2,5-disubstituted iodovinyltetrahydrofurans via the cyclization of γ-silyloxyallenes using n-iodosuccinimide

Sang Wong Kim, R. Walkup, L. Guan, 1992 .

Discovery of potent, selective, and orally bioavailable PDE5 inhibitor: Methyl-4-(3-chloro-4-methoxybenzylamino)-8-(2-hydroxyethyl)-7-methoxyquinazolin-6-ylmethylcarbamate (CKD 533).

S. Ahn, Young Hoon Kim, N. Choi, 2010, Bioorganic & medicinal chemistry letters.

Solid phase synthesis of hydantoin library using a novel cyclization and traceless cleavage step

Jinho Lee, S. Ro, Sang Wong Kim, 1997 .

A Facile Synthesis of 2-Aminothiazolo[5,4-b]-pyridines and 2-Aminobenzoxazoles via Cyclization of Thioureas

G. Han, H. Y. Choo, Sang Wong Kim, 2005 .

Solid-phase combinatorial synthesis and cytotoxicity of 3-aryl-2,4-quinazolindiones.

I. Chung, Sang Kook Lee, M. Kim, 2002, Bioorganic & medicinal chemistry.

Solid phase combinatorial synthesis of benzothiazoles and evaluation of topoisomerase II inhibitory activity.

Sang Kook Lee, G. Han, H. Y. Choo, 2006, Bioorganic & medicinal chemistry.

A Facile Synthesis of 2-Aminothiazolo[5,4-b]pyridines and 2-Aminobenzoxazoles via Cyclization of Thioureas.

G. Han, H. Y. Choo, Sang Wong Kim, 2006 .

Syntheses of the Lower Portions of the Pamamycins from .gamma.-(Silyloxy)allenes Using Stereoselective Cyclization, Reduction, and Aldehyde Addition Methodologies

Sang Wong Kim, R. Walkup, 1994 .

MULTICOMPONENT SOLUTION PHASE SYNTHESIS OF DEHYDROAMINO ACID DERIVATIVES BASED ON THE PASSERINI REACTION

R. W. Armstrong, Sang Wong Kim, Shawn M. Bauer, 1998 .

Solid phase synthesis of benzamidine-derived sulfonamide libraries

Sang Wong Kim, J. Koh, C. Hong, 1997, Molecular Diversity.

Solid phase synthesis of benzamidine and butylamine-derived hydantoin libraries

S. Ro, Sang Wong Kim, J. Koh, 1997, Molecular Diversity.

Syntheses of enantiomerically pure tetrahydrofuran building blocks for nactin and pamamycin antibiotics via an enzymically resolved .gamma.-hydroxyallene

Sang Wong Kim, R. Walkup, S. D. Wagy, 1993 .

Cyclizations of γ-hydroxyallenes mediated by organopalladium halides : a convergent synthetic route to substituted 5-alkenyl-2-furanones and 2-alkenyltetrahydrofurans

M. Mosher, Sang Wong Kim, R. Walkup, 1993 .

An efficient and improved route for the preparation of (S)-5-aminomethyloxazolidinone libraries.

Chung Youl Yoo, D. Lee, Sang Wong Kim, 2004, Journal of combinatorial chemistry.

Access to cis‐2,5‐Disubstituted Iodovinyltetrahydrofurans via the Cyclization of γ‐Silyloxyallenes Using N‐Iodosuccinimide.

Sang Wong Kim, R. Walkup, L. Guan, 1992 .

A palladium-catalyzed cyclization-carbonylation-coupling reaction between aryl halides and γ-Hydroxyallenes to form aryl (tetrahydrofuran-2-yl)vinyl ketones

Sang Wong Kim, R. Walkup, L. Guan, 1995 .

Benzylamine-based selective and orally bioavailable inhibitors of thrombin.

Sangsoo Kim, S. Lee, K. Lee, 1998, Bioorganic & medicinal chemistry letters.

Quinazolines as potent and highly selective PDE5 inhibitors as potential therapeutics for male erectile dysfunction.

S. Ahn, Young Hoon Kim, N. Choi, 2008, Bioorganic & medicinal chemistry letters.