Attempted Heterocyclic Syntheses Through Electrophilic Ring Closure Reactions of 2-Allylaniline Systems Containing Larger Side Chains
- 1 January 1994
- journal article
- research article
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 47 (11) , 2109-2117
- https://doi.org/10.1071/ch9942109
Abstract
The electrophile-initiated cyclization of some 2-allylanilines and their amide derivatives has been further investigated. Although 2-allylanilines with small, allylic substituents such as methyl reacted with iodine to yield 3-iodo-1,2,3,4-tetrahydroquinolines the 2-allylanilines with larger substituents related to those of virantmycin provided low yields of the tetrahydroquinoline as part of a complex product mixture.Keywords
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