X=Y-ZH systems as potential 1,3-dipoles. Part 26. 1,5-electrocyclisation and tandem 1,5-electrocyclisationAldol type condensation processes in imines.
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 46 (5) , 1599-1610
- https://doi.org/10.1016/s0040-4020(01)81969-4
Abstract
No abstract availableThis publication has 41 references indexed in Scilit:
- A Torquospecific 1,5‐ElectrocyclizationHelvetica Chimica Acta, 1987
- Geminale Vinyldiazide, IV1) Substituentenabhängige Konkurrenz zwischen 1,5‐ und 3,5‐Cyclisierung bei Vinylaziden; 1,2,3‐Triazole und 2H‐Azirine aus 3,3‐Diazido‐2‐cyanacrylsäure‐methylester und AminenEuropean Journal of Inorganic Chemistry, 1987
- 1,5‐EIectrocyclization in Homofuran, Homopyrrole, and HomothiopheneAngewandte Chemie International Edition in English, 1987
- 3H-1,3,4-Benzotriazepines from (N-arylbenzimidoyl)-5-dimethylaminotetrazoles: 1,7-vs. 1,5-cyclisation of extended dipolar nitrile iminesJournal of the Chemical Society, Chemical Communications, 1987
- In situ generation of 1,5-dipoles by concerted [1,6] hydrogen transfer. Stereoselective thermal rearrangement of 1-(1-pyrrolidinyl)-1,3-butadienes to pyrrolizinesJournal of the American Chemical Society, 1983
- A 2-Azapentadienyl Carbanion: a Nonstereospecific ElectrocyclizationCanadian Journal of Chemistry, 1975
- 2,4-Diazapentadienes. II. A Carbanion CyclizationCanadian Journal of Chemistry, 1972
- Orbital symmetry in a carbanion cyclizationJournal of the American Chemical Society, 1969
- Kinetics and Mechanism of 1,3‐Dipolar CycloadditionsAngewandte Chemie International Edition in English, 1963
- 1,3‐Dipolar Cycloadditions. Past and FutureAngewandte Chemie International Edition in English, 1963