Practical asymmetric synthetic route to 4,4,4-trifluoro-3-hydroxybutyrate: Head-to-tail and head-to-head crystallizations through double and single hydrogen bonds of hetero- and homochiral 4,4,4-trifluoro-3-hydroxybutyrophenones

Chirality

Volumn 14, Issue 9, 2002, Pages 709-712

  Ishii, Akihiro ^a   Kanai, Masatomi ^b   Higashiyama, Kimio ^c   Mikami, Koichi ^a  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b CENTRAL GLASS CO LTD   (Japan)

^c HOSHI UNIVERSITY   (Japan)

Author keywords

4,4,4 trifluoro 3 hydroxybutyrate; 4,4,4 trifluoro 3 hydroxybutyrophenone; Conglomerate; Heterochiral; Homochiral; Racemate

Indexed keywords

4,4,4 TRIFLUORO 3 HYDROXYBUTYRATE; 4,4,4 TRIFLUORO 3 HYDROXYBUTYROPHENONE; ACETIC ACID DERIVATIVE; BUTYRIC ACID DERIVATIVE; BUTYROPHENONE DERIVATIVE; ESTER DERIVATIVE; PHENYL GROUP; TRIFLUOROPERACETIC ACID; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; CHIRALITY; CRYSTAL STRUCTURE; CRYSTALLIZATION; HYDROGEN BOND; OXIDATION; PRIORITY JOURNAL;

EID: 0036378309     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.10040     Document Type: Article

References (28)

1. Discriminating interactions between chiral molecules
2. Space-group frequencies for organic compounds