Publications by authors named "Guncheol Kim"

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Conversion of oxazolidinediones to isoindoloisoquinolinones via intramolecular Friedel–Crafts reaction.
Ji-Young Min, Guncheol Kim

J Org Chem· February 2014

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Synthesis of amide and urea derivatives of benzothiazole as Raf-1 inhibitor.
Eun Young Song, Navneet Kaur, Mi-Young Park, Yinglan Jin, Kyeong Lee, Guncheol Kim

Eur J Med Chem· July 2008

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Photoreactive immobilization of 11-(2,4-dinitro-5-fluorobenzene)undecenamide on a hydrogenated silicon (100) surface for protein immobilizations.
Tai Hwan Ha, Mi-ra Park, Hye Jung Park, Jae-Sik Choi, Guncheol Kim

Chem Commun (Camb)· April 2007

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New palladium-catalyzed reaction pathway to the Erythrina skeleton.
Guncheol Kim, Jin Hee Kim, Ki Youn Lee

J Org Chem· March 2006

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One-pot hydrogenation conditions for a sequential process to (+)-monomorine.
Guncheol Kim, Sung-Do Jung, Eun-Ju Lee, Nakjeong Kim

J Org Chem· June 2003

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Identification of a novel antiangiogenic agent; 4-(N-imidazol-2-ylmethyl)amino benzopyran analogues.
Nakjeong Kim, Sunkyung Lee, Kyu Yang Yi, Sung-eun Yoo, Guncheol Kim

Bioorg Med Chem Lett· May 2003

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UV band Splitting of chromogenic azo-coupled calix[4]crown upon cation complexation.
Jong Yeol Kim, Guncheol Kim, Chung Ryul Kim, Seoung Ho Lee, Joung Hae Lee, Jong Seung Kim

J Org Chem· March 2003

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Concise Stereoselective Routes to Advanced Intermediates Related to Natural and Unnatural Pinnaic Acid This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154), M.F.H. (5T32 CA62948-05), and D.T. (Schering Research Foundation, Berlin). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses.
Matthew W. Carson, Guncheol Kim, Martin F. Hentemann, Dirk Trauner, Samuel J. Danishefsky

Angew Chem Int Ed Engl· December 2001

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Total Synthesis and Proof of Stereochemistry of Natural and Unnatural Pinnaic Acids: A Remarkable Long-Range Stereochemical Effect in the Reduction of 17-Oxo Precursors of the Pinnaic Acids This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses. We would like to thank professor Nakanishi for his supportive interest in the project.
Matthew W. Carson, Guncheol Kim, Samuel J. Danishefsky

Angew Chem Int Ed Engl· December 2001

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