Novel dipolar cycloaddition reactions of zwitterionic species generated from dimethoxycarbene and dimethyl acetylenedicarboxylate with carbonyl compounds: facile synthesis of dihydrofuran derivatives

Nair, Vijay ; Bindu, S. ; Sreekumar, V. ; Balagopal, Lakshmi (2003) Novel dipolar cycloaddition reactions of zwitterionic species generated from dimethoxycarbene and dimethyl acetylenedicarboxylate with carbonyl compounds: facile synthesis of dihydrofuran derivatives Synthesis, 2003 (9). pp. 1446-1456. ISSN 0039-7881

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Official URL: https://www.thieme-connect.com/ejournals/abstract/...

Related URL: http://dx.doi.org/10.1055/s-2003-40192

Abstract

The reaction of 1:1 zwitterionic species, generated in situ by the addition of dimethoxycarbene to dimethyl acetylenedicarboxylate, towards carbonyl compounds is described. The reactions presented offer a one-pot synthesis of dihydrofuran and spiro dihydrofuran derivatives in high yields.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Aldehydes; Carbenes; Nucleophilic Additions; Ketones; Quinones
ID Code:58046
Deposited On:31 Aug 2011 12:45
Last Modified:31 Aug 2011 12:45

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