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2,4,6-Tri-tert-butylphenyl and 2,4-di-tert-butyl-6-methylphenyl groups: Look similar, react differently

✍ Scribed by Alex S. Ionkin; William J. Marshall


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
137 KB
Volume
13
Category
Article
ISSN
1042-7163

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✦ Synopsis


Abstract

The crystal structures of molecules with two phosphaalkene groups have been determined. Differences in the stabilization of the Pο£ΎC π‐bond by the 2,4,6‐tri‐tert‐butylphenyl and 2,4‐di‐tert‐butyl‐6‐methylphenyl groups were observed. It has been found that lithium supermesityl(trimethylsilyl)phosphide could be a very efficient base to remove a proton from acetonitrile.Β© 2002 Wiley Periodicals, Inc. Heteroatom Chem 13:662–666, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10083


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