ELECTROCYCLIZATION OF 3-AZAHEXA-1,3,5-TRIENES - A CONVENIENT IMINOPHOSPHORANE-MEDIATED PREPARATION OF 4-ARYLPYRIDINES

Citation
P. Molina et al., ELECTROCYCLIZATION OF 3-AZAHEXA-1,3,5-TRIENES - A CONVENIENT IMINOPHOSPHORANE-MEDIATED PREPARATION OF 4-ARYLPYRIDINES, Tetrahedron letters, 34(23), 1993, pp. 3773-3776
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
34
Issue
23
Year of publication
1993
Pages
3773 - 3776
Database
ISI
SICI code
0040-4039(1993)34:23<3773:EO3-AC>2.0.ZU;2-9
Abstract
Aza Wittig reaction of iminophosphoranes 1, derived from alpha-azido-a lpha,beta-unsaturated esters and beta-arylpropenals 2 leads to 4-arylp yridines in moderate to good yields.