Issue 11, 1972
From the journal:

Journal of the Chemical Society, Chemical Communications

The question of quasi-enamine reactivity of aminocyclopropanes. Rearrangement of isomeric 1-(morpholino)-7-chloro-7-phenylbicyclo[4,1,0]heptanes

U. K. Pandit  and  S. A. G. de Graaf  

Abstract

Comparison of the course of thermal rearrangement of isomeric chlorobicycloheptanes (1) and (2) reveals that the formation of products from (2) can be interpreted in terms of “quasi-enamine” reactivity.

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Article information

DOI
https://doi.org/10.1039/C39720000659
Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 659-660

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The question of quasi-enamine reactivity of aminocyclopropanes. Rearrangement of isomeric 1-(morpholino)-7-chloro-7-phenylbicyclo[4,1,0]heptanes

U. K. Pandit and S. A. G. de Graaf, J. Chem. Soc., Chem. Commun., 1972, 659 DOI: 10.1039/C39720000659

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