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(1): 27-28
DOI: 10.1055/s-1996-5322
DOI: 10.1055/s-1996-5322
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.
Base-Mediated Ring-Opening Reactions of Episulfones to give Alkenylsulfinates: A Stereoselective Synthesis of Alkenyl Sulfones
Further Information
Publication History
Publication Date:
31 December 2000 (online)
A range of episulfones undergo ring-opening to give alkenylsulfinates on treatment with LDA in THF. The sulfinates can then be alkylated with a number of alkyl halides to give alkenyl sulfone products in a stereoselective fashion.
episulfone - ring-opening - alkenyl sulfone