Resolution of 2-chloromandelic acid with (R)-(+)-N-benzyl-1- phenylethylamine: Chiral discrimination mechanism

Chirality

Volumn 24, Issue 5, 2012, Pages 349-355

  Peng, Yangfeng ^a   He, Quan ^b   Rohani, Sohrab ^b   Jenkins, Hilary ^c  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b UNIVERSITY OF WESTERN ONTARIO   (Canada)

^c MCMASTER UNIVERSITY   (Canada)

Author keywords

(R) (+) N benzyl 1 phenylethylamine; 2 chloromandelic acid; CH interaction; chiral discrimination; chiral recognition; crystallization resolution; diastereomeric salt; hydrogen bond; van der Waals

Indexed keywords

2 CHLOROMANDELIC ACID; AMINE; MANDELIC ACID DERIVATIVE; N BENZYL 1 PHENYLETHYLAMINE; SODIUM CHLORIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; CHIRALITY; CRYSTAL STRUCTURE; HYDROGEN BOND; HYDROPHOBICITY; PRIORITY JOURNAL;

BENZYL COMPOUNDS; CRYSTALLOGRAPHY, X-RAY; ETHYLAMINES; HYDROGEN BONDING; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MANDELIC ACIDS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PHENETHYLAMINES; SOLUBILITY; STEREOISOMERISM; TRANSITION TEMPERATURE;

EID: 84860488157     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.22013     Document Type: Article

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