Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Wayne J, Thompson"'
Publikováno v:
Tetrahedron letters. 32(41)
An efficient and stereocontrolled synthesis of various C2-symmetric HIV-l protease inhibitors is described, starting from commercially available and inexpensive D-mannitol.
Publikováno v:
Tetrahedron letters. 33(20)
An efficient and mild method for alkoxycarbonylation of amines is described, utilizing commercially available N,N'-disuccinimidyl carbonate.
Publikováno v:
The Journal of organic chemistry. 58(5)
The synthesis of a differentially protected dipeptide mimic 10 in enantiomerically pure form is described. The key step involves the epimerization of the C-2 center of the lactone 4, hydrolysis and protection of the resulting hydroxy acid, followed b
Autor:
Theodore P. Broten, Wayne J. Thompson, Hee Yoon Lee, Ann L. Scott, Jill M. Erb, Joel R. Huff, Terry W. Schorn, Jennie B. Nerenberg, Raymond S.L. Chang, Tsing B. Chen, James P. Guare, Stacey O'Malley, Peter M. Munson, Jeffrey M. Bergman
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 8:2467-2472
Benign prostatic hyperplasia can be managed pharmacologically with alpha-1 adrenergic receptor antagonists. Agents that demonstrate selectivity for the alpha-1a receptor subtype may offer advantages in clinical applications with respect to hypotensiv
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:83-88
Cyclic sulfone-3-carboxamides are effective P2-1igands for HIV-1 protease inhibitors. Incorporation of 3S-tetrahydro-2H-thiopyrancarboxamide-l, l-dioxide in the hydroxyethylamine series resulted in inhibitor 14 (IC50=9 nM, CIC95=200 nM) with improved
Autor:
Arun K. Ghosh, Wayne J. Thompson, M. Katharine Holloway, Sean P. McKee, Tien T. Duong, Hee Yoon Lee, Peter M. Munson, Anthony M. Smith, Jenny M. Wai, Paul L. Darke, Joan A. Zugay, Emilio A. Emini, William A. Schleif, Joel R. Huff, Paul S. Anderson
Publikováno v:
Journal of Medicinal Chemistry. 36:2300-2310
A series of protease inhibitors bearing constrained unnatural amino acids at the P2-position and novel heterocycles at the P3-position of compound 1 (Ro 31-8959) were synthesized, and their in vitro enzyme inhibitory and antiviral activities were eva
Autor:
Arun K. Ghosh, S. P. Mckee, T. T. Duong, Emilio A. Emini, William A. Schleif, Peter M. Munson, Zugay Ja, Paul L. Darke, Hee Yoon Lee, Wayne J. Thompson
Publikováno v:
Journal of Medicinal Chemistry. 36:924-927
Autor:
Kensaku Nakayama, Wayne J. Thompson
Publikováno v:
ChemInform. 22
A general methodology for the preparation of both enantiomers of a variety of trialkyl phosphates with enantiomeric excesses ranging from 87 to 92% is described. Bis(2,4-dichlorophenyl) phosphoramidates bearing a 2-substituted pyrrolidine moiety as t
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 23
The palladium catalyzed coupling of allylic acetates with carbon nucleophiles generates urethane protected trans-allylic amines with exceptionally high stereoselectivity.