C. J. Lim

发表

2-Heteroaryl Benzimidazole Derivatives as Melanin Concentrating Hormone Receptor 1 (MCH-R1) Antagonists

K. Yi, B. Lee, Kwang-Seok Oh, 2013 .

Predicted Ligands for the Human Urotensin‐II G Protein‐Coupled Receptor with Some Experimental Validation

W. Goddard, K. Yi, B. Trzaskowski, 2014, ChemMedChem.

2‐Heteroaryl Benzimidazole Derivatives as Melanin Concentrating Hormone Receptor 1 (MCH‐R1) Antagonists.

K. Yi, B. Lee, Kwang-Seok Oh, 2013 .

Synthesis and SAR of 5-aryl-furan-2-carboxamide derivatives as potent urotensin-II receptor antagonists.

K. Yi, Hye-Jin Park, B. Lee, 2019, Bioorganic & medicinal chemistry letters.

Indole‐2‐carboxamide Derivatives as Potent Urotensin‐II Receptor (UT) Antagonists

K. Yi, B. Lee, Kwang-Seok Oh, 2017 .

A urotensin II receptor antagonist, KR36676, decreases vascular remodeling and inflammation in experimental pulmonary hypertension.

K. Yi, J. H. Lee, H. Seo, 2016, International immunopharmacology.

Synthesis and SAR of thieno[3,2-b]pyridinyl urea derivatives as urotensin-II receptor antagonists.

K. Yi, B. Lee, Kwang-Seok Oh, 2014, Bioorganic & medicinal chemistry letters.

The orally active urotensin receptor antagonist, KR36676, attenuates cellular and cardiac hypertrophy

C. H. Park, K. Yi, H. Seo, 2015, British journal of pharmacology.

KR-39038, a Novel GRK5 Inhibitor, Attenuates Cardiac Hypertrophy and Improves Cardiac Function in Heart Failure

K. Yi, J. H. Lee, H. Seo, 2020, Biomolecules & therapeutics.

4-Aminophthalazin-1(2H)-one Derivatives as Melanin Concentrating Hormone Receptor 1 (MCH-R1) Antagonists

K. Yi, Nakjeong Kim, B. Lee, 2013 .

Synthesis and SAR study of pyrrolo[3,4-b]pyridin-7(6H)-one derivatives as melanin concentrating hormone receptor 1 (MCH-R1) antagonists.

K. Yi, Ji Young Kim, B. Lee, 2013, Bioorganic & medicinal chemistry letters.

4-arylphthalazin-1(2H)-one derivatives as potent antagonists of the melanin concentrating hormone receptor 1 (MCH-R1).

K. Yi, B. Lee, Kwang-Seok Oh, 2012, Bioorganic & medicinal chemistry letters.

Benzo[b]thiophene-2-carboxamide derivatives as potent urotensin-II receptor antagonists.

Simon S. Woo, K. Yi, B. Lee, 2016, Bioorganic & medicinal chemistry letters.

1,3,4‐Thiadiazol‐2‐amine Derivatives as Urotensin‐II Receptor (UT) Antagonists

K. Yi, B. Lee, Kwang-Seok Oh, 2015 .

Decarboxylative Allylation and Vinylation Approach of Thiohydroxamate Esters

C. J. Lim, Sunggi Lee, Sunggak Kim, 2004 .

Tin-free Radical Acylation Reactions Using Alkyl Allyl Sulfones as Radical Precursors

C. J. Lim, Sunggak Kim, 2003 .

Decarboxylative acylation approach of thiohydroxamate esters

Han-young Kang, C. J. Lim, Sunggak Kim, 2001 .

Tin-Free Radical-Mediated CC-Bond Formations with Alkyl Allyl Sulfones as Radical Precursors†

C. J. Lim, Sunggak Kim, Chae Jo Lim, 2002 .

Radical-mediated gamma-functionalizations of alpha,beta-unsaturated carboxylic amides.

C. J. Lim, Sunggak Kim, 2004, Angewandte Chemie.

Novel radical alkylation of carboxylic imides.

C. J. Lim, Changsik Song, Sunggak Kim, 2002, Journal of the American Chemical Society.

Beta-elimination of a phosphonate group from an alkoxy radical: an intramolecular acylation approach using an acylphosphonate as a carbonyl group acceptor.

Chang Ho Cho, C. J. Lim, Sunggak Kim, 2003, Journal of the American Chemical Society.

Enantioselective conjugate radical addition to alpha'-hydroxy enones.

Rajesh Subramaniam, M. Sibi, C. J. Lim, 2006, Organic letters.

Radical-Mediated?-Functionalizations ofa,-Unsaturated Carboxylic Amides

C. J. Lim, Sunggak Kim, 2005 .