STEREOSPECIFIC PICTET-SPENGLER REACTION - SYNTHESIS OF CIS (-(1S,12BR)-1-AMINOINDOLOQUINOLIZIDINE FROM A PURE ALPHA-(S)-AMINOALDEHYDE DERIVATIVE())

Authors
MELNYK P DUCROT P THAL C
Citation
P. Melnyk et al., STEREOSPECIFIC PICTET-SPENGLER REACTION - SYNTHESIS OF CIS (-(1S,12BR)-1-AMINOINDOLOQUINOLIZIDINE FROM A PURE ALPHA-(S)-AMINOALDEHYDE DERIVATIVE()), Tetrahedron, 49(38), 1993, pp. 8589-8596
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
49
Issue
38
Year of publication
1993
Pages
8589 - 8596
Database
ISI
SICI code
0040-4020(1993)49:38<8589:SPR-SO>2.0.ZU;2-S
Abstract
Pictet-Spengler reaction provides cis (+)-1-(S)-aminoindolo[2,3-a]quin olizidine in an enantio- and diastereoselective manner, using an alpha -aminoaldehyde derived from L-glutamic acid.