Chiral cinchona alkaloid-derived thiourea catalyst for enantioselective synthesis of novel β-amino esters by Mannich reaction

Chirality

Volumn 24, Issue 3, 2012, Pages 223-231

  Li, Weihua ^a   Song, Baoan ^a   Bhadury, Pinaki S ^a   Li, Liang ^a   Wang, Zhenchao ^a   Zhang, Xiaoyan ^a   Hu, Deyu ^a   Chen, Zhuo ^a   Zhang, Yuping ^a   Bai, Song ^a   Wu, Jian ^a   Yang, Song ^a  

^a GUIZHOU UNIVERSITY   (China)

Author keywords

asymmetric amino esters; benzothiazole moiety; chiral cinchona alkaloid derived thiourea; enantiomeric excess

Indexed keywords

BENZOTHIAZOLE; CINCHONA ALKALOID; DIETHYL 2 [[4 METHYLBENZO(D)THIAZOL 2 YLAMINO)(2 CHLOROPHENYL) METHYL]MALONATE; DIETHYL 2 [[4 METHYLBENZO(D)THIAZOL 2 YLAMINO)(4 CHLOROPHENYL)METHYL]MALONATE; DIETHYL 2 [[4 METHYLBENZO(D)THIAZOL 2 YLAMINO](2 FLUOROPHENYL)METHYL]MALONATE; DIETHYL 2 [[4 METHYLBENZO(D)THIAZOL 2 YLAMINO](4 FLUOROPHENYL)METHYL]MALONATE; DIETHYL 2 [[4METHYLBENZO(D)THIAZOL 2 YLAMINO](PHENYL)METHYL] MALONATE; DIETHYL 2 [[6 METHOXYBENZO(D)THIAZOL 2 YLAMINO] (2 CHLOROPHENYL)METHYL]MALONATE; DIETHYL 2 [[6 METHOXYBENZO(D)THIAZOL 2 YLAMINO] (4 CHLOROPHENYL)METHYL]MALONATE; DIETHYL 2 [[6 METHOXYBENZO(D)THIAZOL 2 YLAMINO] (4 FLUOROPHENYL)METHYL]MALONATE; DIETHYL 2 [[6 METHOXYBENZO(D)THIAZOL 2 YLAMINO](2 FLUOROPHENYL)METHYL]MALONATE; DIETHYL 2 [[6 METHOXYBENZO(D)THIAZOL 2 YLAMINO](PHENYL)METHYL]MALONATE; IMINE; MALONIC ACID; QUINIDINE; QUININE; THIOUREA; UNCLASSIFIED DRUG;

AMINO ACID SYNTHESIS; ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CHIRALITY; COLUMN CHROMATOGRAPHY; ENANTIOMER; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MANNICH REACTION; MELTING POINT; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

CATALYSIS; CHEMISTRY TECHNIQUES, SYNTHETIC; CINCHONA ALKALOIDS; ESTERS; MANNICH BASES; STEREOISOMERISM; SUBSTRATE SPECIFICITY; THIOUREA;

EID: 84862777255     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.21986     Document Type: Article

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