Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 1996; 1996(7): 655-656
DOI: 10.1055/s-1996-5562
DOI: 10.1055/s-1996-5562
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Elimination of vic-Disulfonates Using Sodium Hydrogen Telluride in Dimethylformamide
Further Information
Publication History
Publication Date:
31 December 2000 (online)
Sodium hydrogen telluride in DMF reacts efficiently with vic-disulfonates to give alkenes in a stereospecific manner. Threo-isomers yielded the trans-alkenes only while erythro-isomers gave the cis-alkenes.
Alkenes - disulfonates - stereospecific - diol - tellurium