1,3-DIPOLAR CYCLOADDITION REACTIONS OF CYCLOOCTYNE WITH AZOMETHINE YLIDES

Authors
MATSUMOTO K OHTA R UCHIDA T NISHIOKA H YOSHIDA M KAKEHI A
Citation
K. Matsumoto et al., 1,3-DIPOLAR CYCLOADDITION REACTIONS OF CYCLOOCTYNE WITH AZOMETHINE YLIDES, Journal of heterocyclic chemistry, 32(1), 1995, pp. 367-369
Citations number
17
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of heterocyclic chemistry → ACNP
ISSN journal
0022152X
Volume
32
Issue
1
Year of publication
1995
Pages
367 - 369
Database
ISI
SICI code
0022-152X(1995)32:1<367:1CROCW>2.0.ZU;2-7
Abstract
Cyclooctyne smoothly underwent 1,3-dipolar cycloaddition with aziridin es and pyridinium ylides to afford the corresponding pyrroles and indo lizines in moderate to good yields.