Stereoselective synthesis of dipeptide β-turn mimetics: 7-Benzyl and 8-phenyl substituted azabicyclo[4.3.0]nonane amino acid esters

Journal of Organic Chemistry

Volumn 67, Issue 18, 2002, Pages 6353-6360

  Wang, Wei ^a,b   Yang, Jianqing ^a   Ying, Jinfa ^a   Xiong, Chiyi ^a   Zhang, Junyi ^a   Cai, Chaozhong ^a   Hruby, Victor J ^a  

^a University of Arizona   (United States)

^b GENOMICS INSTITUTE OF THE NOVARTIS RESEARCH FOUNDATION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

STEREOSELECTIVE METHOD;

AMINO ACIDS; CATALYSIS; HYDROGENATION; SYNTHESIS (CHEMICAL);

AROMATIC COMPOUNDS;

ALPHA AMINO ACID; AZABICYCLO[4.3.0]NONANE AMINO ACID ESTER; BETA LACTAM DERIVATIVE; DIPEPTIDE; ESTER; PYROGLUTAMIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; DIASTEREOISOMER; HYDROGENATION; PROTEIN STRUCTURE; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

AMINO ACIDS; AZA COMPOUNDS; BICYCLO COMPOUNDS; CATALYSIS; COMBINATORIAL CHEMISTRY TECHNIQUES; CYCLIZATION; ESTERS; INDICATORS AND REAGENTS; MOLECULAR MIMICRY; MOLECULAR STRUCTURE; PEPTIDES; PROTEIN CONFORMATION; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0037031636     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0203591     Document Type: Article

References (40)