SYNTHESIS OF ENANTIOMERICALLY PURE HETEROCYCLES - ACCESS TO HYDROXYLATED PIPERIDINES FROM A SUGAR LACTONE

Authors
THOMASSIGNY C BENNIS K GELAS J
Citation
C. Thomassigny et al., SYNTHESIS OF ENANTIOMERICALLY PURE HETEROCYCLES - ACCESS TO HYDROXYLATED PIPERIDINES FROM A SUGAR LACTONE, Synthesis, (2), 1997, pp. 191
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthesis → ACNP
ISSN journal
00397881
Issue
2
Year of publication
1997
Database
ISI
SICI code
0039-7881(1997):2<191:SOEPH->2.0.ZU;2-M
Abstract
A protected hydroxylated piperidine 7 and its bicyclo- and substituted diastereoisomers 12 and 13, respectively, have been synthesized from alpha-D-isosaccharino-1,4-lactone (3), in two very short sequences.