ETUDE DE LA REACTIVITE DE L'ION AZOTURE VIS A VIS DE CATIONS HETEROCYCLIQUES-IV COMPORTEMENT VIS A VIS DE CATIONS CHROMYLIUM DIVERSEMENT SUBSTITUES. REARRANGEMENT THERMIQUE DES AZIDES COVALENTS OBTENUS. VOIE ORIGINALE D'ACCES AUX BENZHETEROAZEPINES

DOI: 10.1016/S0040-4020(01)91509-1

Source and publish data:

Tetrahedron p. 3567 - 3577 (1984)

Update date:2022-08-04

Topics: ion azoture cations hétérocycliques azides covalents

Authors:

Desbene, P.-L.

Cherton, J.-C.

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Article abstract of DOI:10.1016/S0040-4020(01)91509-1

The study of the azide nucleophile reaction with substituted chromylium salts is presented.When heated, the azido 2H-and azdo 4H-chromenes obtained give benz(f)oxazepins in very good yields.This is an easy preparation of these compounds.

Full text of DOI:10.1016/S0040-4020(01)91509-1

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