C. Gilley

发表

New entry to convertible isocyanides for the Ugi reaction and its application to the stereocontrolled formal total synthesis of the proteasome inhibitor omuralide.

Yoshihisa Kobayashi, M. J. Buller, C. Gilley, 2007, Organic letters.

Synthesis and SAR of b-annulated 1,4-dihydropyridines define cardiomyogenic compounds as novel inhibitors of TGFβ signaling.

J. Cashman, M. Mercola, D. Schade, 2012, Journal of medicinal chemistry.

Synthesis of Proteasome Inhibitor Omuralide Featuring Stereocontrolled Ugi Reaction and Novel Convertible Isocyanide

Yoshihisa Kobayashi, M. J. Buller, C. Gilley, 2009 .

2-nitrophenyl isocyanide as a versatile convertible isocyanide: rapid access to a fused gamma-lactam beta-lactone bicycle.

Yoshihisa Kobayashi, C. Gilley, 2008, The Journal of organic chemistry.

Expeditious access to unprotected racemic pyroglutamic acids.

Yoshihisa Kobayashi, C. Gilley, J. Isaacson, 2007, The Journal of organic chemistry.

The Oxidation of Primary Alcohols to Methyl Esters and Diols to Lactones Using Trichloroisocyanuric Acid

C. Gilley, G. A. Hiegel, 2003 .

Nerve agent analogues that produce authentic soman, sarin, tabun, and cyclohexyl methylphosphonate-modified human butyrylcholinesterase.

J. Cashman, O. Lockridge, L. Schopfer, 2009, Chemical research in toxicology.

Chemical synthesis of two series of nerve agent model compounds and their stereoselective interaction with human acetylcholinesterase and human butyrylcholinesterase.

Nora H Barakat, J. Cashman, Shubham Vyas, 2009, Chemical research in toxicology.

1,5-Disubstituted benzimidazoles that direct cardiomyocyte differentiation from mouse embryonic stem cells.

J. Cashman, M. Mercola, P. Bushway, 2015, Bioorganic & medicinal chemistry.

Vesicular transport of fe and interaction with other metal ions in polarized Caco2 cell monolayers.

M. Linder, C. Gilley, Mizue Moriya, 2006, Biological research.