Nucleophilic Displacement Reactions of Halogenated Cyclobutenes1
JD Park, LH Wilson, JR Lacher
Index: Park,J.D. et al. Journal of Organic Chemistry, 1963 , vol. 28, p. 1008 - 1012
Full Text: HTML
Citation Number: 10
Abstract
Recent investigations concerning nucleophilic displacement reactions of halogenated cyclobutenes have shown that these cyclobutenes readily undergo reaction with nucleophilic reagents with and without rearrangement. In niost studies, 2-6 the cyclobutenes possessed highly activated double bonds or groups attached thereon capable of stabilizing a charge. For this work, a series of halogenated cyclobutenes, namely 3, 3, 4, 4-tetrafluoro ...
Related Articles:
Synthesen von Moniliformin, einem Mycotoxin mit Cyclobutendion??Struktur
[Bellus; Fischer; Greuter; Martin Helvetica Chimica Acta, 1978 , vol. 61, # 5 p. 1784 - 1813]