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

Bibliographical note

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

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/S0040-4039(00)86404-7

Cite this

@article{6c61c04a25ce49d69af57f8fc652af9a,

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",

doi = "10.1016/S0040-4039(00)86404-7",

language = "English",

volume = "24",

pages = "1201--1204",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "11",

}

TY - JOUR

T1 - X=Z-ZH systems as potential 1,3-dipoles. 1,5-electrocyclisatioins of imines

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.

UR - http://www.scopus.com/inward/record.url?scp=49049124955&partnerID=8YFLogxK

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

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

M3 - Article

AN - SCOPUS:49049124955

VL - 24

SP - 1201

EP - 1204

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 11

ER -

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

Abstract

Bibliographical note

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this