Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jag P, Heer"'
Publikováno v:
Western Journal of Emergency Medicine, Vol 13, Iss 1, Pp 125-126 (2012)
[West J Emerg Med. 2012;13(1):125–126.]
Externí odkaz:
https://doaj.org/article/188c7beaef2244d985a7725ca02095c4
Publikováno v:
Journal of medicinal chemistry. 61(10)
Tackling PPIs, particularly by stabilizing clinically favored conformations of target proteins, with orally available, bona fide small molecules remains a significant but immensely worthwhile challenge for the pharmaceutical industry. Success may be
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 153:247-258
Catalytic enantioselective oxidation of a range of sulfides is achieved in very high yields by treatment with hydrogen peroxide in conjunction with enantiomerically pure sulfonylimines under basic conditions. Enantioselectivities of up to ca. 98% or
Publikováno v:
Tetrahedron: Asymmetry. 6:2911-2914
[(3,3-Dimethoxycamphoryl)sulfonyl]oxaziridine oxidizes sulfides to sulfoxides cleanly and efficiently in up to 98% ee.
Publikováno v:
Tetrahedron Letters. 35:9629-9632
Catalytic asymmetric oxidation of sulfides is achieved in a remarkably simple process by treatment with hydrogen peroxide and an enantiomerically pure sulfonylimine under basic conditions.
Autor:
B. K. Park, Philip C. Bulman Page, O. Markopoulou, Jag P. Heer, Donald Bethell, Andrew E. Graham
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 26
Catalytic asymmetric oxidation of sulfides is achieved in a remarkably simple process by treatment with hydrogen peroxide and an enantiomerically pure sulfonylimine under basic conditions.
Publikováno v:
ChemInform. 26
Publikováno v:
ChemInform. 27
[(3,3-Dimethoxycamphoryl)sulfonyl]oxaziridine oxidizes sulfides to sulfoxides cleanly and efficiently in up to 98% ee.
Autor:
Paul A. Stocks, Hooshang Vahedi, Mark Healy, Eric W. Collington, David M. Andrews, Jag P. Heer, Andrew E. Graham, Donald Bethell, Philip C. Bulman Page
Publikováno v:
ChemInform. 29