Abstract
The naphthylidene imine of methyl (1-cyclopentenyl)glycine undergoes competitive double bond isomerization and 1,5-electrocyclisation via a dipolar tautomer.
Original language | English |
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Pages (from-to) | 1201-1204 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 24 |
Issue number | 11 |
DOIs | |
Publication status | Published - 1983 |
Bibliographical note
Copyright:Copyright 2014 Elsevier B.V., All rights reserved.
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry