ASYMMETRIC-SYNTHESIS OF ,8,8A,9-HEXAHYDRO-1-ALKYLPYRROLO[3,2-F]INDOLIZINES VIA INTRAMOLECULAR IMINIUM ION CYCLIZATION

Authors
ANNUNZIATA R FERRARI M PAPEO G RESMINI M SISTI M
Citation
R. Annunziata et al., ASYMMETRIC-SYNTHESIS OF ,8,8A,9-HEXAHYDRO-1-ALKYLPYRROLO[3,2-F]INDOLIZINES VIA INTRAMOLECULAR IMINIUM ION CYCLIZATION, Synthetic communications, 27(1), 1997, pp. 23-38
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthetic communications → ACNP
ISSN journal
00397911
Volume
27
Issue
1
Year of publication
1997
Pages
23 - 38
Database
ISI
SICI code
0039-7911(1997)27:1<23:AO,>2.0.ZU;2-A
Abstract
Enantiomerically pure compounds embodying the 4,6,7,8,8a,9-hexahydropy rrolo[3,2-f]indolizine unit were synthesized via intramolecular iminiu m ion cyclization. An improved procedure for the preparation of the ox azolidinone 1 is also reported.