InCl3-catalyzed [3+ 2] cycloaddition reactions: a facile synthesis of trans-dihydrobenzofurans and substituted cyclobutane derivatives

Yadav, J. S. ; Reddy, B. V. S. ; Kondaji, G. (2003) InCl3-catalyzed [3+ 2] cycloaddition reactions: a facile synthesis of trans-dihydrobenzofurans and substituted cyclobutane derivatives Synthesis, 2003 (7). pp. 1100-1104. ISSN 0039-7881

Full text not available from this repository.

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

Related URL: http://dx.doi.org/10.1055/s-2003-39175

Abstract

1,4-Benzoquinones undergo smoothly [3 + 2] cycloaddition reactions with electron rich alkenes in the presence of 10 mol% indium trichloride or 5 mol% iodine under mild conditions to afford the corresponding 2,3-dihydrobenzofurans in excellent yields with trans-selectivity. Similarly, methyl vinyl ketone reacts with electron rich olefins to produce substituited trans-cyclobutane derivatives.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Indium Reagents; Iodine; P-quinones; Alkenes; Benzofurans
ID Code:63139
Deposited On:28 Sep 2011 03:20
Last Modified:28 Sep 2011 03:20

Repository Staff Only: item control page