76989-79-2Relevant articles and documents
1-Naphthylpropargyl ether group: A readily cleaved and sterically minimal protecting system for stereoselective glycosylation
Crich, David,Wu, Baolin
, p. 4879 - 4882 (2007/10/03)
(Chemical Equation Presented) The (1-naphthyl)propargyl group is introduced as a sterically unobtrusive alcohol protecting group that is cleaved in a single step by exposure to dichlorodicyanoquinone in wet dichloromethane. In conjunction with the 4,6-O-b
The preparation of β-hydroxysulfoxides
Gabbi, Cristina,Ghelfi, Franco,Grandi, Romano
, p. 2857 - 2863 (2007/10/03)
Oxidation of β-hydroxy thioethers with MnO2-aqu.35%/HCl in methanol gives β-hydroxy sulfoxides in high yields.
Stereoselektive Synthese von Alkoholen; V. Einfache regioselektive Umwandlung von Alkyl-ketonen in Allylalkohole
Goldmann, Siegfried
, p. 640 - 642 (2007/10/02)
-
