Y. C. Kim

发表

Palladium-catalyzed vinylic substitution reactions with heterocyclic bromides

W. Frank, R. Heck, Y. C. Kim, 1978 .

A highly efficient synthesis of unnatural l-sugars from d-ribose

H. Moon, W. J. Choi, L. Jeong, 2005 .

Total synthesis of 8-oxypseudopalmatine and 8-oxypseudoberberine via ring-closing metathesis

Yong‐Chul Kim, W. Cho, D. B. Khadka, 2009 .

Photoaddition reactions of acenaphthylenedione with .alpha.-silyl n-electron donors via triplet single electron transfer desilylation and triplet hydrogen atom abstraction pathways

U. Yoon, P. Mariano, Donguk Kim, 1992 .

Total Synthesis of Sanjoinine-G1

Hyun-Ok Yang, Jeong-Hill Park, Y. Kang, 1995 .

Crystallization and Preliminary X-Ray Crystallographic Studies of Rattus norvegicus Visfatin/PBEF/Nampt in Complex with an FK866-Based Inhibitor

S. Eom, Yongseong Kim, Jang-Soo Chun, 2009 .

Structure−Activity Relationship Studies of Spinorphin as a Potent and Selective Human P2X3 Receptor Antagonist

Yong‐Chul Kim, Chul-Seung Park, Hyun-Ho Lim, 2007 .

Anilide derivatives of an 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A(2B) adenosine receptors.

K. Jacobson, J. Linden, X. Ji, 2000, Journal of medicinal chemistry.

Derivatives of the triazoloquinazoline adenosine antagonist (CGS15943) are selective for the human A3 receptor subtype.

K. Jacobson, X. Ji, Y. C. Kim, 1996, Journal of medicinal chemistry.

Synthesis and Structure—Activity Relationships of Pyrazolodiazepine Derivatives as Human P2X7 Receptor Antagonists.

Ju-Yeon Lee, Juan Yu, W. Cho, 2010 .

Corrigendum to “Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor” [Bioorg. Med. Chem. Lett. 18 (2008) 571–575]

K. Jacobson, H. Moon, L. Jeong, 2009 .

[3H]MRS 1754, a selective antagonist radioligand for A(2B) adenosine receptors.

K. Jacobson, J. Linden, X. Ji, 2001, Biochemical pharmacology.