Publications by authors named "Jerry Murry"

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Human therapies as a successful liaison between chemistry and biology.
Patrick A Baeuerle, Jerry A Murry

Chem Biol· September 2014

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Iodide-catalyzed reductions: development of a synthesis of phenylacetic acids.
Jacqueline E Milne, Thomas Storz, John T Colyer, Oliver R Thiel, Mina Dilmeghani Seran, Jerry A Murry

J Org Chem· November 2011

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Practical syntheses of a CXCR3 antagonist.
Johann Chan, Brenda J Burke, Kyle Baucom, Karl Hansen, Matthew M Bio, Jerry Murry

J Org Chem· March 2011

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Asymmetric synthesis of a potent, aminopiperidine-fused imidazopyridine dipeptidyl peptidase IV inhibitor.
Feng Xu, Edward Corley, Michael Zacuto, David A Conlon, Brenda Pipik, Jerry Murry

J Org Chem· March 2010

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An efficient and scalable Ritter reaction for the synthesis of tert-butyl amides.
Jean C Baum, Jacqueline E Milne, Jerry A Murry, Oliver R Thiel

J Org Chem· March 2009

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Pd-catalyzed deoxygenation of mandelate esters.
Jacqueline E Milne, Jerry A Murry, Anthony King, Robert D Larsen

J Org Chem· January 2009

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A case of remote asymmetric induction in the peptide-catalyzed desymmetrization of a bis(phenol).
Chad A Lewis, Jeffrey L Gustafson, Anna Chiu, Jaume Balsells, David Pollard, Jerry Murry

J Am Chem Soc· December 2008

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Discovery of a stable molecular complex of an API with HCl: a long journey to a conventional salt.
Andrey Peresypkin, Narayan Variankaval, Russell Ferlita, Robert Wenslow, Jacqueline Smitrovich, Jerry Murry

J Pharm Sci· September 2008

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Chlorination/cyclodehydration of amino alcohols with SOCl2: an old reaction revisited.
Feng Xu, Bryon Simmons, Robert A Reamer, Edward Corley, Jerry Murry

J Org Chem· January 2008

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Rh(II)-catalyzed intermolecular oxidative sulfamidation of aldehydes: a mild efficient synthesis of N-sulfonylcarboxamides.
Johann Chan, Kyle D Baucom, Jerry A Murry

J Am Chem Soc· November 2007

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An efficient and scalable synthesis of substituted phenanthrenequinones by intramolecular Friedel-Crafts reaction of imidazolides.
Naoki Yoshikawa, Austin Doyle, Lushi Tan, Jerry A Murry, Atsushi Akao

Org Lett· October 2007

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Highly selective cascade couplings for the syntheses of functionalized piperidinones and bispidines.
Feng Xu, Edward Corley, Jerry A Murry, David M Tschaen

Org Lett· July 2007

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Novel intramolecular reactivity of oximes: synthesis of cyclic and spiro-fused imines.
Cécile G Savarin, Christiane Grisé, Jerry A Murry, Robert A Reamer, David L Hughes

Org Lett· March 2007

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Remote desymmetrization at near-nanometer group separation catalyzed by a miniaturized enzyme mimic.
Chad A Lewis, Anna Chiu, Michele Kubryk, Jaume Balsells, David Pollard, Jerry Murry

J Am Chem Soc· December 2006

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Stereocontrolled synthesis of trisubstituted cyclopropanes: expedient, atom-economical, asymmetric syntheses of (+)-Bicifadine and DOV21947.
Feng Xu, Jerry A Murry, Bryon Simmons, Edward Corley, Kenneth Fitch

Org Lett· August 2006

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Direct N-acetyl enamine formation: lithium bromide mediated addition of methyllithium to nitriles.
Cécile G Savarin, Geneviève N Boice, Jerry A Murry, Edward Corley, Lisa DiMichele

Org Lett· August 2006

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Practical preparation of 3,3-difluoropyrrolidine.
Feng Xu, Bryon Simmons, Joseph Armstrong, Jerry Murry

J Org Chem· July 2005

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Direct synthesis of 4-arylpiperidines via palladium/copper(I)-cocatalyzed Negishi coupling of a 4-piperidylzinc iodide with aromatic halides and triflates.
Edward G Corley, Karen Conrad, Jerry A Murry, Cecile Savarin, Justin Holko

J Org Chem· July 2004

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Improved carbonylation of heterocyclic chlorides and electronically challenging aryl bromides.
Jennifer Albaneze-Walker, Charles Bazaral, Tanya Leavey, Peter G Dormer, Jerry A Murry

Org Lett· June 2004

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Synthesis of substituted imidazoles via organocatalysis.
Doug E Frantz, Louis Morency, Arash Soheili, Jerry A Murry, Edward J J Grabowski

Org Lett· March 2004

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Michael reactions of pseudoephedrine amide enolates: effect of LiCl on syn/anti selectivity.
Jacqueline H Smitrovich, Lisa DiMichele, Chuanxing Qu, Geneviève N Boice, Todd D Nelson, Jerry Murry

J Org Chem· March 2004

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Synthetic methodology utilized to prepare substituted imidazole p38 MAP kinase inhibitors.
Jerry A Murry

Curr Opin Drug Discov Devel· November 2003

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Efficient and general protocol for the copper-free sonogashira coupling of aryl bromides at room temperature.
Arash Soheili, Jennifer Albaneze-Walker, Jerry A Murry, Peter G Dormer, David L Hughes

Org Lett· October 2003

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A convenient one-pot synthesis of 1,8-naphthyridones.
Shawn A Springfield, Karen Marcantonio, Scott Ceglia, Jennifer Albaneze-Walker, Peter G Dormer, Jerry A Murry

J Org Chem· May 2003

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An expedient synthesis of highly functionalized naphthyridones and quinolines from a common N-aryl pyridinone template.
Cécile G Savarin, Jerry A Murry, Peter G Dormer

Org Lett· June 2002

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