The cyclisation of benzonitrile 3,3-diarylallyl ylides to give 3H-2-benzazepines: Substituent directive effects and mechanism
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (18) , 2069-2072
- https://doi.org/10.1016/s0040-4039(00)96047-7
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Carbenic reactions of 4-diazo-4-imidazole with benzene derivativesTetrahedron Letters, 1986
- The photochemical reactions of α,β,γ,δ -unsaturated diazo compounds at low temperatureTetrahedron, 1984
- A study of periselectivity in the thermal cyclisation reactions of diene-conjugated diazo compounds: 1,7-cyclisation as a route to 3H-1,2-diazepines and 1,5-cyclisation leading to new rearrangement reactions of 3H-pyrazolesTetrahedron, 1984
- Photochemical transformations of small ring heterocyclic systems. LXV. Intramolecular cycloaddition reactions of vinyl-substituted 2H-azirinesJournal of the American Chemical Society, 1975
- Steric effects in the cyclisation of diazoalkenes: a new route to 1,2-benzodiazepinesJournal of the Chemical Society D: Chemical Communications, 1970