Increasing chiral recognition in acetal formation

Chirality

Volumn 21, Issue 4, 2009, Pages 428-435

  Noe, Christian R ^a   Knollmüller, Max ^b   Jangg, Edith ^b   Gmeiner, Günter P ^c   Urban, Ernst ^a   Eppacher, Simon ^a  

^a UNIVERSITY OF VIENNA   (Austria)

^b VIENNA UNIVERSITY OF TECHNOLOGY   (Austria)

^c Seibersdorf Labor GmbH   (Austria)

Author keywords

Acetal formation; Resolution of racemic carbinols; Selective lactols

Indexed keywords

ACETAL; LACTONE; METHYL GROUP; SULFANILAMIDE;

ACETALIZATION; ARTICLE; BROMINATION; CHEMICAL ANALYSIS; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; CHIRALITY; ENANTIOSELECTIVITY; MOLECULAR RECOGNITION; PRIORITY JOURNAL; RACEMIC MIXTURE; REDUCTION; SAPONIFICATION; SUBSTITUTION REACTION; SULFONATION; SYNTHESIS;

ACETALS; CHEMISTRY; CHEMISTRY, ORGANIC; GLUCOSE; LACTONES; LIGANDS; MODELS, CHEMICAL; MODELS, MOLECULAR; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; STEREOISOMERISM; SULFONAMIDES;

EID: 65549131582     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20609     Document Type: Article

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