Iminium ion route to azomethine yields from primary and secondary amines
- 1 January 1986
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 8,p. 602-604
- https://doi.org/10.1039/c39860000602
Abstract
Iminium ion formation between primary or secondary amines and carbonyl compounds containing the moiety OC–CX results in a facile and stereospecific generation of azomethine yields which can be trapped in 1,3-dipolar cycloaddition reactions.Keywords
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