Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Viktor O. Rogatchov"'
Publikováno v:
Chinese Journal of Chemistry. 24:681-688
Asymmetric epoxidation of N-enoylsultams (1, 3–15) incorporating a variety of chiral sultams as the chiral induction elements with UHP/TFAA has been studied. Both diastereomeric isomers of epoxides (2, 16–28) were obtained in high yield and moder
Autor:
Birgit Wibbeling, Viktor O. Rogatchov, Peter Metz, Pia Schwab, Roland Fröhlich, Heiko Bernsmann
Publikováno v:
Tetrahedron Letters. 43:4753-4756
Enantiomerically pure δ- and γ-sultams have been prepared by intramolecular [4+2] cycloaddition of N-1-phenylethyl substituted vinylsulfonamides with purely thermal activation and under high pressure. An optimized procedure for reductive debenzylat
Autor:
Birgit Wibbeling, Heiko Bernsmann, Pia Schwab, Peter Metz, Viktor O. Rogatchov, Roland Froehlich
Publikováno v:
ChemInform. 33
Publikováno v:
ChemInform. 37
Asymmetric epoxidation of N-enoylsultams (1, 3–15) incorporating a variety of chiral sultams as the chiral induction elements with UHP/TFAA has been studied. Both diastereomeric isomers of epoxides (2, 16–28) were obtained in high yield and moder
Autor:
Albert W. M. Lee, Shu Jia Zhang, Wing Hong Chan, Viktor O. Rogatchov, Peter Metz, Wai Yeung Wong
Publikováno v:
Journal of Chemical Research. 2005:755-756
Diastereomeric isomers of epoxides 15-28 are obtained in high yield and moderate to high optical purity when N-enoylsultams 1-14 incorporating a variety of chiral sultams as the chiral induction elements are treated with urea-hydrogen peroxide/triflu