S. Kang

发表

Synthesis of pyridazine and thiazole analogs as SGLT2 inhibitors.

Jinhwa Lee, S. Kang, K. Song, 2010, Bioorganic & medicinal chemistry.

Design and synthesis of novel arylpiperazine derivatives containing the imidazole core targeting 5-HT(2A) receptor and 5-HT transporter.

Min Ju Kim, Jinhwa Lee, H. Seo, 2011, Journal of medicinal chemistry.

1,2,4-Triazinylmethylphenyl Glucoside as Novel C-Aryl Glucoside SGLT2 Inhibitors

Min Ju Kim, S. Kang, Jin Hwa Lee, 2011 .

Novel C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents: Pyridazinylmethylphenyl glucoside congeners.

Min Ju Kim, J. Lee, Jinhwa Lee, 2010, Bioorganic & medicinal chemistry letters.

Glucosides with cyclic diarylpolynoid as novel C-aryl glucoside SGLT2 inhibitors.

Min Ju Kim, Jinhwa Lee, S. Kang, 2011, Bioorganic & Medicinal Chemistry Letters.

Pentacycle derivatives as cannabinoid CB1 receptor ligands.

Min Ju Kim, Jinhwa Lee, Kwangwook Ahn, 2009, Bioorganic & medicinal chemistry letters.

Oxadiazole-diarylpyrazole 4-carboxamides as cannabinoid CB1 receptor ligands.

Min Ju Kim, Jinhwa Lee, H. Seo, 2009, Bioorganic & medicinal chemistry letters.

Enantioselective iodocyclization and mercuriocyclization of γ-hydroxy-cis-alkenes

Mihyong Kim, S. Kang, C. Park, 2005 .

Catalytic asymmetric mercuriocyclization of gamma-hydroxy-cis-alkenes.

Mihyong Kim, S. Kang, S. Kang, 2004, Angewandte Chemie.

Further optimization of novel pyrrole 3-carboxamides for targeting serotonin 5-HT(2A), 5-HT(2C), and the serotonin transporter as a potential antidepressant.

Min Ju Kim, A. Pae, Jinhwa Lee, 2010, Bioorganic & medicinal chemistry.

Total synthesis of natural tert-alkylamino hydroxy carboxylic acids.

Hee-Seung Lee, S. Kang, A. J. Buglass, 2005, Chemical reviews.

Biarylpyrazolyl oxadiazole as potent, selective, orally bioavailable cannabinoid-1 receptor antagonists for the treatment of obesity.

Chong-Hwan Chang, Hyun-Ju Park, H. Yun, 2008, Journal of medicinal chemistry.

Total Synthesis of Natural tert‐Alkylamino Hydroxy Carboxylic Acids

Hee-Seung Lee, S. Kang, A. J. Buglass, 2006 .

Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyrazol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist.

Min Ju Kim, J. Lee, H. Seo, 2010, Bioorganic & medicinal chemistry.

Tetrazole-biarylpyrazole derivatives as cannabinoid CB1 receptor antagonists.

Jinhwa Lee, Kwangwook Ahn, H. Seo, 2008, Bioorganic & medicinal chemistry letters.

Total synthesis of natural (+)-lasonolide A.

S. Kang, C. Park, S. Kang, 2003, Angewandte Chemie.

Stereoselective Total Synthesis of the Natural (+)-Lasonolide A

S. Kang, J. Youn, S. Kang, 2004 .

A stereoselective synthesis of the C15–C25 subunit of (+)-lasonolide A

S. Kang, J. Youn, S. Kang, 2003 .

Total Synthesis of Natural (+)-Lasonolide A (I).

S. Kang, C. Park, S. Kang, 2004 .

Arylpiperazine-containing pyrrole 3-carboxamide derivatives targeting serotonin 5-HT(2A), 5-HT(2C), and the serotonin transporter as a potential antidepressant.

Min Ju Kim, A. Pae, Jinhwa Lee, 2010, Bioorganic & medicinal chemistry letters.

Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyrazol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist.

Min Ju Kim, J. Lee, H. Seo, 2010, Bioorganic & medicinal chemistry.