Elucidation of chiral recognition mechanism during preferential and diastereomeric crystallizations, and application to the development and utilization of artificial enantiopure compounds

Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry

Volumn 64, Issue 12, 2006, Pages 1240-1250

  Saigo, Kazuhiko ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

Asymmetric synthesis; CH interaction; Chiral polyamide; Diastereomeric crystallization; Non natural chiral auxiliaries; Phosphonothioic and phosphinothioic acids; Preferential crystallization; Relative molecular length; Three component crystal

Indexed keywords

CARBOXYLIC ACIDS; MOLECULAR STRUCTURE; POLYIMIDES; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

ASYMMETRIC SYNTHESIS; CH/Π INTERACTION; CHIRAL POLYAMIDE; DIASTEREOMERIC CRYSTALLIZATION; MOLECULAR LENGTH; NON-NATURAL CHIRAL AUXILIARIES; PHOSPHINOTHIOIC ACIDS; PREFERENTIAL CRYSTALLIZATION; RELATIVE MOLECULAR LENGTH; THREE-COMPONENT CRYSTAL;

CRYSTALLIZATION;

EID: 33847778427     PISSN: 00379980     EISSN: None     Source Type: Journal    
DOI: 10.5059/yukigoseikyokaishi.64.1240     Document Type: Article

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