|
Volumn 57, Issue 30, 2001, Pages 6417-6427
|
Synthesis of constrained prolines by Diels-Alder reaction using a chiral unsaturated oxazolone derived from (R)-glyceraldehyde as starting material
|
Author keywords
Amino acids; Asymmetric synthesis; Constrained pralines; Diastereoselective Diels Alder reactions
|
Indexed keywords
2 PROPYL 7 AZABICYCLO[2.2.1]HEPTANE 1 CARBOXYLIC ACID;
7 AZABICYCLO[2.2.1]HEPTANE 1,2 DICARBOXYLIC ACID;
ALKADIENE;
ASPARTIC ACID DERIVATIVE;
CARBOXYLIC ACID DERIVATIVE;
GLYCERALDEHYDE;
METHYL N BENZOYL 2 (1,2 DIHYDROXYETHYL) 7 AZABICYCLO[2.2.1]HEPTANE 1 CARBOXYLATE;
METHYL N BENZOYL 2 (2,2 DIMETHYL 1,3 DIOXOLAN 4 YL) 7 AZABICYCLO[2.2.1]HEPTANE 1 CARBOXYLATE;
METHYL N BENZOYL 2 FORMYL 7 AZABICYCLO[2.2.1]HEPTANE 1 CARBOXYLATE;
METHYL N BENZOYL 2 PROPYL 7 AZABICYCLO[2.2.1]HEPTANE 1 CARBOXYLATE;
N BENZOYL 1 CARBOMETHOXY 7 AZABICYCLO[2.2.1]HEPTANE 2 CARBOXYLIC ACID;
NORLEUCINE;
OXAZOLONE;
PROLINE DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL REACTION;
CHIRALITY;
CYCLIZATION;
DRUG CONFORMATION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENANTIOMER;
METHODOLOGY;
PRIORITY JOURNAL;
REACTION ANALYSIS;
BETULACEAE;
|
EID: 0035939192
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/S0040-4020(01)00533-6 Document Type: Article |
Times cited : (28)
|
References (73)
|