STEREOCONTROLLED ADDITION OF PI-TYPE NUCLEOPHILES TO A BICYCLIC N-ACYLIMINIUM ION - NEW ACCESS TO TRANS-2,6-DISUBSTITUTED PIPERIDINE SUBSTRUCTURES

Authors
DAVID M DHIMANE H VANUCCIBACQUE C LHOMMET G
Citation
M. David et al., STEREOCONTROLLED ADDITION OF PI-TYPE NUCLEOPHILES TO A BICYCLIC N-ACYLIMINIUM ION - NEW ACCESS TO TRANS-2,6-DISUBSTITUTED PIPERIDINE SUBSTRUCTURES, Synlett, (2), 1998, pp. 206
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
2
Year of publication
1998
Database
ISI
SICI code
0936-5214(1998):2<206:SAOPNT>2.0.ZU;2-P
Abstract
Bicyclic N-acyliminium ion I, generated in situ by treatment of aminoe ther 4 with Lewis acids, smoothly reacted with pi-type nucleophiles, l eading exclusively to the trans adducts.