A convenient route to enantiopure 3-aryl-2,3-diaminopropanoic acids by diastereoselective Mannich reaction of camphor-based tricyclic iminolactone with imines

Journal of Organic Chemistry

Volumn 73, Issue 9, 2008, Pages 3634-3637

  Zhang, Huan Huan ^a   Hu, Xiu Qin ^a   Wang, Xiao ^a   Luo, Yong Chun ^a   Xu, Peng Fei ^a  

^a LANZHOU UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOMERS; ORGANIC ACIDS; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

ASYMMETRIC SYNTHESIS; DIAMINOPROPANOIC ACIDS; MANNICH REACTION;

ESTERS;

CAMPHOR; IMINE; LACTONE DERIVATIVE; POLYPEPTIDE ANTIBIOTIC AGENT; PROPIONIC ACID DERIVATIVE; TETRAHYDROFURAN;

ADDUCTION; ANTIFUNGAL ACTIVITY; ANTIMICROBIAL ACTIVITY; ARTICLE; ASYMMETRIC SYNTHESIS; CHEMICAL BOND; CHEMICAL STRUCTURE; CHIRALITY; COLUMN CHROMATOGRAPHY; DRUG USE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; ISOMER; ISOMERISM; MANNICH REACTION; NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; X RAY CRYSTALLOGRAPHY;

BETA-ALANINE; CAMPHOR; HETEROCYCLIC COMPOUNDS, 3-RING; HYDROLYSIS; IMINES; LACTONES; MANNICH BASES; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 43449120404     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8001408     Document Type: Article

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