X=Y-ZH SYSTEMS AS POTENTIAL 1,3-DIPOLES. 1,5-ELECTROCYCLISATIONS OF IMINES

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

Source and publish data:

Tetrahedron Letters p. 1201 - 1204 (1983)

Update date:2022-08-05

Topics:

Authors:

Grigg, R.

Gunaratne, H. Q. N.

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Article abstract of DOI:10.1016/S0040-4039(00)86404-7

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

Full text of DOI:10.1016/S0040-4039(00)86404-7

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