J. A. Ray

发表

AN UNCONVENTIONAL ULTRA-HIGH VACUUM FACILITY

C. F. Barnett, J. A. Ray, 1965 .

Delineation of the recharge area for Rio Springs, Kentucky: an EPA demonstration project in wellhead (Springhead) protection for karst terranes

J. A. Ray, G. M. Schindel, J. F. Quinlan, 1996 .

A Novel Family of Small Cysteine-rich Antimicrobial Peptides from Seed of Impatiens balsamina Is Derived from a Single Precursor Protein*

I. J. Evans, J. A. Ray, W. Broekaert, 1997, The Journal of Biological Chemistry.

Substrate specificity in short-chain phospholipid analogs at the active site of human synovial phospholipase A2.

J. A. Ray, M. Lambert, S. Blanchard, 1994, Journal of medicinal chemistry.

Synthesis of ultra-short-acting neuromuscular blocker GW 0430: a remarkably stereo- and regioselective synthesis of mixed tetrahydroisoquinolinium chlorofumarates.

J. A. Ray, R. Mook, V. Samano, 1999, Organic letters.

Enzymatic- and iridium-catalyzed asymmetric synthesis of a benzothiazepinylphosphonate bile acid transporter inhibitor.

J. A. Ray, Amy A Sarjeant, J. Collins, 2013, The Journal of organic chemistry.

6-Azasteroids: structure-activity relationships for inhibition of type 1 and 2 human 5 alpha-reductase and human adrenal 3 beta-hydroxy-delta 5-steroid dehydrogenase/3-keto-delta 5-steroid isomerase.

J. A. Ray, S. Frye, R. Mook, 1994, Journal of medicinal chemistry.

Novel, potent P2-P3 pyrrolidine derivatives of ketoamide-based cathepsin K inhibitors.

J. A. Ray, L. Shewchuk, A. Hassell, 2006, Bioorganic & medicinal chemistry letters.

Synthesis of 1-aminocyclopropenecarboxylic acid: the unsaturated analog of ACC

J. A. Ray, T. Wheeler, 1987 .

A Convenient and Efficient Synthesis of 1-Aminocyclopropanecarboxylic Acid (ACC)

J. A. Ray, T. Wheeler, 1988 .

Stereocontrolled synthesis of cis-dibenzoquinolizine chlorofumarates: curare-like agents of ultrashort duration.

J. A. Ray, R. Mook, A. Sefler, 2001, The Journal of organic chemistry.

Neuromuscular blocking activity and therapeutic potential of mixed-tetrahydroisoquinolinium halofumarates and halosuccinates in rhesus monkeys.

Sanjay S. Patel, J. A. Ray, R. Mook, 2003, Journal of medicinal chemistry.

Bis- and mixed-tetrahydroisoquinolinium chlorofumarates: new ultra-short-acting nondepolarizing neuromuscular blockers.

J. A. Ray, R. Mook, V. Samano, 1999, Journal of medicinal chemistry.

Pyrazolopyridine antiherpetics: SAR of C2' and C7 amine substituents.

J. A. Ray, V. Samano, G. A. Freeman, 2005, Bioorganic & medicinal chemistry.

Novel arylsulfonamides possessing sub-picomolar HIV protease activities and potent anti-HIV activity against wild-type and drug-resistant viral strains.

J. A. Ray, M. Hanlon, E. Furfine, 2004, Bioorganic & medicinal chemistry letters.

P2-P3 conformationally constrained ketoamide-based inhibitors of cathepsin K.

J. A. Ray, L. Shewchuk, A. Hassell, 2005, Bioorganic & medicinal chemistry letters.

Preparation of enol lactones of 3,5,7-triketo and 3,5,7,9-tetraketo acids by the condensation of 4,6-dimethoxy-2-pyrone with anions of mono- and diketones

J. A. Ray, T. Harris, 1982 .

Nucleophilic attack on 4,6-dimethoxy-2-pyrones; discovery of a remarkably facile rearrangement of the pyrones

J. A. Ray, T. Harris, J. Cha, 1989 .

Synthesis and biological activity of a novel series of indole-derived PPARγ agonists

Steven G. Blanchard, John A. Ray, Rayomand J. Unwalla, 1999 .

Synthesis of novel anilinoquinolines as c-fms inhibitors.

J. A. Ray, L. Frick, V. Samano, 2007, Bioorganic & medicinal chemistry letters.