Lewis acid catalyzed 1,3-dipolar cycloadditon reactions of stabilized azomethine ylides

Authors
Dogan, O Koyuncu, H Kaniskan, U
Citation
O. Dogan et al., Lewis acid catalyzed 1,3-dipolar cycloadditon reactions of stabilized azomethine ylides, TURK J CHEM, 25(3), 2001, pp. 365-371
Citations number
35
Categorie Soggetti
Chemistry
Journal title
TURKISH JOURNAL OF CHEMISTRY
ISSN journal
13000527 → ACNP
Volume
25
Issue
3
Year of publication
2001
Pages
365 - 371
Database
ISI
SICI code
1300-0527(2001)25:3<365:LAC1CR>2.0.ZU;2-A
Abstract
Diethylzinc was tested for the first time as the Lewis acid in 1,3-dipolar cycloaddition reactions of azomethine ylides to synthesize pyrrolidine deri vatives. A new, easily applicable and highly selective method was developed for the synthesis of highly substituted pyrrolidines. By the application o f this method, the synthesis of three new pyrrolidine derivatives was achie ved.