Enamines. Part XXXVIII. Configurations of 1-aryl-1-dialkylaminopropenes

1 January 1974

journal article
research article
Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1

p. 2671-2672
https://doi.org/10.1039/p19740002671

Abstract

The configurations of several 1-aryl-1-dialkylaminopropenes have been assigned from ¹H n.m.r. data. The olefinic protons of the E-isomers resonate at higher field than those of the corresponding Z-isomers.

Keywords

PART XXXVIII
ARYL
CONFIGURATIONS
ENAMINES
1H N.M.R
OLEFINIC PROTONS
CORRESPONDING Z
Z ISOMERS
FIELD THAN

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