X=Z-ZH systems as potential 1,3-dipoles. 1,5-electrocyclisatioins of imines

R. Griss; H. Q.N. Gunaratne

doi:10.1016/S0040-4039(00)86404-7

X=Z-ZH systems as potential 1,3-dipoles. 1,5-electrocyclisatioins of imines

R. Griss^*, H. Q.N. Gunaratne

^*Corresponding author for this work

School of Chemistry and Chemical Engineering

Research output: Contribution to journal › Article › peer-review

17 Citations (Scopus)

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
Pages (from-to)	1201-1204
Number of pages	4
Journal	Tetrahedron Letters
Volume	24
Issue number	11
DOIs	https://doi.org/10.1016/S0040-4039(00)86404-7
Publication status	Published - 1983

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Copyright 2014 Elsevier B.V., All rights reserved.

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)86404-7

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title = "X=Z-ZH systems as potential 1,3-dipoles. 1,5-electrocyclisatioins of imines",

abstract = "The naphthylidene imine of methyl (1-cyclopentenyl)glycine undergoes competitive double bond isomerization and 1,5-electrocyclisation via a dipolar tautomer.",

author = "R. Griss and Gunaratne, {H. Q.N.}",

year = "1983",

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AU - Griss, R.

AU - Gunaratne, H. Q.N.

PY - 1983

Y1 - 1983

N2 - The naphthylidene imine of methyl (1-cyclopentenyl)glycine undergoes competitive double bond isomerization and 1,5-electrocyclisation via a dipolar tautomer.

AB - The naphthylidene imine of methyl (1-cyclopentenyl)glycine undergoes competitive double bond isomerization and 1,5-electrocyclisation via a dipolar tautomer.

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U2 - 10.1016/S0040-4039(00)86404-7

DO - 10.1016/S0040-4039(00)86404-7

M3 - Article

AN - SCOPUS:49049124955

SN - 0040-4039

VL - 24

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EP - 1204

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 11

ER -

X=Z-ZH systems as potential 1,3-dipoles. 1,5-electrocyclisatioins of imines

Abstract

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