Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: The stereochemistry of the adducts derived from the Diels-Alder addition of cyclobutenes and cyclopentadienones: a caveat on some existing PMR methods for the assignment of stereochemistry
Author: Warrener, R.N.
Tan, R.Y.S.
Russell, R.A.
Citation: Tetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1979; 20(31):2943-2946
Publisher: Pergamon Press
Issue Date: 1979
ISSN: 0040-4039
Statement of
Ronald N. Warrener, Richard Y.S. Tan, Richard A. Russell
Abstract: The stereochemistry of the adducts formed from the cycloaddition of tetracyclone, phencyclone and 2-methyl-3,4,5-triphenylcyclopenta-2,4-dienone with cis-3,4-dichlorocyclobutene (in one case with 3-chloro-4-methoxycyclobutene) has been evaluated in a rigorous fashion. This allows a firmly-based caveat to be issued regarding the p.m.r. probe for stereochemical evaluation of tetracyclone adducts recently proposed by Coxon and Battiste.
Rights: © Pergamon Press Ltd. 1979.
DOI: 10.1016/S0040-4039(01)86459-5
Appears in Collections:Aurora harvest 7
Chemistry publications

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.