|
Volumn , Issue 18, 2011, Pages 2697-2700
|
A highly efficient conversion of a simple derivative of the amino acid proline into a nearly enantiomerically pure n-protected allyl amine: Use of thionyl chloride to promote the Peterson olefination
|
Author keywords
allylamines; amino acids; chiral pool; olefination; pyrrolidines
|
Indexed keywords
ALDEHYDE;
ALKENE;
ALLYLAMINE DERIVATIVE;
BETA HYDROXYSILANE;
CARBOXYLIC ACID DERIVATIVE;
CHLORIDE;
GRIGNARD REAGENT;
PROLINE;
PYRROLIDINE DERIVATIVE;
SILANE DERIVATIVE;
TERT BUTYL 2 [1 HYDROXY(TRIMETHYLSILYL)ETHYL]PYRROLIDINE 1 CARBOXYLATE;
TERT BUTYL 2 VINYLPYRROLIDINE 1 CARBOXYLATE;
THIONYL CHLORIDE;
UNCLASSIFIED DRUG;
VINYLPYRROLIDINE;
ACIDITY;
ALKALINITY;
AMINO ACID ANALYSIS;
ARTICLE;
CHEMICAL COMPOSITION;
CHEMICAL INTERACTION;
CHEMICAL STRUCTURE;
CONTROLLED STUDY;
ENANTIOMER;
OLEFINATION;
PETERSON OLEFINATION;
PURIFICATION;
RACEMIZATION;
STEREOCHEMISTRY;
STRUCTURE ACTIVITY RELATION;
WITTIG REACTION;
|
EID: 80455160072
PISSN: 09365214
EISSN: 14372096
Source Type: Journal
DOI: 10.1055/s-0031-1289536 Document Type: Article |
Times cited : (4)
|
References (35)
|