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 1992; 1992(1): 25-26
DOI: 10.1055/s-1992-21252
DOI: 10.1055/s-1992-21252
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.
Radical Isomerization and Allylation Reactions of 2-Iodo-3,3-dimethyl-4-pentenoate Esters
Further Information
Publication History
Publication Date:
18 September 2002 (online)

Sunlamp irradiation of methyl 2-iodo-3,3-dimethyl-4-pentenoate (2c) induces isomerization to an equilibrium mixture rich (13/1) in methyl 3-iodo-3-methyl-2-vinylbutanoate (3c). Allylations of 2c with allyl sulfides and stannanes produce mixtures of rearranged (9; 6-substituted 3-methoxycarbonyl-4,4-dimethyl-1,6-heptadienes) or unrearranged (8; 6-substituted 4-methoxycarbonyl-3,3-dimethyl-1,6- heptadienes) allylation products.