AN EFFICIENT SYNTHESIS OF 1,2,3,4-TETRASUBSTITUTED PYRROLES VIA INTRAMOLECULAR AZOMETHINE YLIDE [3-DIPOLAR CYCLOADDITION(2])

Authors
TOYOTA M NISHIKAWA Y FUKUMOTO K
Citation
M. Toyota et al., AN EFFICIENT SYNTHESIS OF 1,2,3,4-TETRASUBSTITUTED PYRROLES VIA INTRAMOLECULAR AZOMETHINE YLIDE [3-DIPOLAR CYCLOADDITION(2]), Heterocycles, 39(1), 1994, pp. 39-42
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Heterocycles → ACNP
ISSN journal
03855414
Volume
39
Issue
1
Year of publication
1994
Pages
39 - 42
Database
ISI
SICI code
0385-5414(1994)39:1<39:AESO1P>2.0.ZU;2-C
Abstract
A sequence of reactions, involving intramolecular azomethine ylide [32] dipolar cycloaddition, was used to efficiently construct 1,2,3,4-te trasubstituted pyrroles.