Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elisabeth A. Schmittling"'
Autor:
Elisabeth A. Schmittling, William T. Jackson, J. Scott Sawyer, David L. Saussy, S. Richard Baker, Philip Marder, Bach Nicholas J, Larry L. Froelich
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:2077-2082
We report the preparation and pharmacologic activity of three spatial analogues of LY292728, a highly potent xanthone dicarboxylic LTB4 receptor antagonist. Molecular modeling of these compounds has helped to further elucidate the nature of the secon
Autor:
Jason Scott Sawyer, Floreancig Paul Edward, D. L. Jun. Saussy, Carlos R. Roman, Peter W. Stengel, Larry L. Froelich, Jerome H. Fleisch, Michael J. Sofia, Bach Nicholas J, Stephen Richard Baker, Sandra L. Cockerham, Stephen M. Spaethe, P. Marder, Elisabeth A. Schmittling, Baldwin Rf, J. A. Palkowitz, P. S. Borromeo, William T. Jackson, Steven A. Silbaugh
Publikováno v:
ChemInform. 27
Publikováno v:
ChemInform. 30
Publikováno v:
Tetrahedron Letters. 32:7207-7210
The use of potassium fluoride on basic alumina in acetonitrile with ultrasound for the selecting deprotection of tert -butyldimethylsilyl ethers of phenols is described. The method, which features a non-aqueous work-up, readily cleaves tert- butyldim
Publikováno v:
The Journal of organic chemistry. 63(18)
An efficient alternative to the Ullmann ether synthesis of diaryl ethers, diaryl thioethers, and diarylamines involving the S(N)Ar addition of a phenol, thiophenol, or aniline to an appropriate aryl halide, mediated by potassium-fluoride alumina and
Publikováno v:
The Journal of Organic Chemistry. 58:3229-3230
An efficient alternative to the copper-catalyzed synthesis (Ullmann ether synthesis) of diaryl ethers, diaryl thioethers, and diarylamines involving the potassium fluoride-alumina-mediated addition of a phenol, thiophenol, or an aniline to 2- or 4-fl