W. Jung

发表

Total synthesis and biological evaluation of C16 analogs of (-)-dictyostatin.

B. Day, D. Curran, Y. Shin, 2007, Journal of medicinal chemistry.

Efficacious and orally bioavailable thrombin inhibitors based on a 2,5-thienylamidine at the P1 position: discovery of N-carboxymethyl-d-diphenylalanyl-l-prolyl[(5-amidino-2-thienyl)methyl]amide.

C. Park, Sang Kook Lee, Sun Hwa Lee, 2003, Journal of medicinal chemistry.

Noncovalent thrombin inhibitors incorporating an imidazolylethynyl P1.

S. Lee, K. Lee, W. Jung, 2000, Bioorganic & medicinal chemistry letters.

Noncovalent tripeptidic thrombin inhibitors incorporating amidrazone, amine and amidine functions at P1.

C. Park, Sun Hwa Lee, W. Jung, 2002, Bioorganic & medicinal chemistry letters.

Fluorobenzamidrazone thrombin inhibitors: influence of fluorine on enhancing oral absorption.

S. Lee, S. Hwang, K. Lee, 1999, Bioorganic & medicinal chemistry letters.

Confirmation of the stereostructure of (+)-cytostatin by fluorous mixture synthesis of four candidate stereoisomers.

D. Curran, Shuichi Nakamura, J. Mancuso, 2008, Angewandte Chemie.

Catalytic asymmetric allylation of aldehydes with BINOL-Ti(IV) complex accelerated by i-PrSSiMe3

W. Jung, Ha-soon Choi, C.‐M. Yu, 1996 .

Effects of Subjoin Lewis Acid on the Catalytic Asymmetric Allylic Transfer Reactions of Aldehydes Promoted by BINOL-Ti(IV) Complex

Sook-Kyung Yoon, W. Jung, Ha-soon Choi, 1997 .

Streamlined syntheses of (-)-dictyostatin, 16-desmethyl-25,26-dihydrodictyostatin, and 6-epi-16-desmethyl-25,26-dihydrodictyostatin.

B. Day, D. Curran, R. Balachandran, 2010, Journal of the American Chemical Society.

Diastereoselective synthesis of highly functionalized tetrahydropyrans from the cyclic vinyl acetal with aldehydes mediated by lewis acid catalyst

W. Jung, Ha-soon Choi, Chan-Mo Yu, 1995 .

Bifunctional molecular accelerator for catalytic asymmetricallylation: R2MSR′ (M = B, Al) as a useful synergeticreagent

Jaewook Shin, W. Jung, Ha-soon Choi, 1997 .

Self-regulated molecular rearrangement: diastereoselective zwitterionic aza-Claisen protocol

W. Jung, Ha-soon Choi, C.‐M. Yu, 1996 .

AN EFFICIENT ONE POT SYNTHESIS OF N,N-DISUBSTITUTED UNSYMMETRICAL UREAS AND CARBAMATES

C. Park, Ho-il Choi, K. Moon, 1996 .

Benzylamine-based selective and orally bioavailable inhibitors of thrombin.

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

Noncovalent Tripeptidic Thrombin Inhibitors Incorporating Amidrazone, Amine, and Amidine Functions at P1

C. Park, Sun Hwa Lee, W. Jung, 2002 .

Cell-Based and Biochemical Structure-Activity Analyses of Analogs of the Microtubule Stabilizer Dictyostatin

B. Day, D. Curran, Y. Fukui, 2008, Molecular Pharmacology.

Improved synthesis of 6-epi-dictyostatin and antitumor efficacy in mice bearing MDA-MB231 human breast cancer xenografts.

B. Day, D. Curran, J. Eiseman, 2008, Journal of medicinal chemistry.

Effects of Subjoin Lewis Acid on the Catalytic Asymmetric Allylic Transfer Reactions of Aldehydes Promoted by BINOL-Ti(IV) Complex

Sook-Kyung Yoon, W. Jung, Ha-soon Choi, 1997 .

Streamlined syntheses of (-)-dictyostatin, 16-desmethyl-25,26-dihydrodictyostatin, and 6-epi-16-desmethyl-25,26-dihydrodictyostatin.

B. Day, D. Curran, R. Balachandran, 2010, Journal of the American Chemical Society.

Confirmation of the stereostructure of (+)-cytostatin by fluorous mixture synthesis of four candidate stereoisomers.

D. Curran, Shuichi Nakamura, J. Mancuso, 2008, Angewandte Chemie.