๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Regio- and Stereospecific Ring Opening of 1,1-Dialkyl-2-(aryloxymethyl)aziridinium Salts by Bromide.

โœ Scribed by Matthias D'hooghe; Veronique Van Speybroeck; Michel Waroquier; Norbert De Kimpe

Publisher
John Wiley and Sons
Year
2006
Weight
22 KB
Volume
37
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Opposite Regioselectivity in the Sequent
Opposite Regioselectivity in the Sequential Ring-Opening of 2-(Alkanoyloxymethyl)aziridinium Salts by Bromide and Fluoride in the Synthesis of Functionalized ฮฒ-Fluoro Amines.
โœ Matthias D'hooghe; Norbert De Kimpe ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons โš– 21 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Ring-opening of epoxyalcohols by diethyl
Ring-opening of epoxyalcohols by diethylaluminium cyanide. Regio- and stereoselective synthesis of 1-cyano-2,3-diols
โœ Fabio Benedetti; Federico Berti; Stefano Norbedo ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 211 KB

Diethylaluminium cyanide is a highly selective reagent for the ring opening of 2,3-epoxyalcohols under mild conditions; the reaction takes place at C-3, with inversion of configuration, to give 1-cyano-2,3-diols.