VCD spectroscopic investigation of enantiopure cyclic β-lactams obtained through lipolase-catalyzed enantioselective ring-opening reaction

Chirality

Volumn 18, Issue 9, 2006, Pages 733-740

  Vass, Elemér ^a   Hollósi, Miklós ^a,b   Forró, Eniko ^c   Fülöp, Ferenc ^c  

^a EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^b INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^c UNIVERSITY OF SZEGED   (Hungary)

Author keywords

lactams; Absolute configuration; Conformation; H bonded dimers; Vibrational circular dichroism (VCD)

Indexed keywords

AMIDE; AMINO ACID DERIVATIVE; BETA AMINO ACID; BETA LACTAM DERIVATIVE; CHLOROFORM; ENZYME; LIPOLASE; ORGANIC SOLVENT; UNCLASSIFIED DRUG;

AB INITIO CALCULATION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHIRALITY; CIRCULAR DICHROISM; CONFORMATIONAL TRANSITION; ENANTIOSELECTIVITY; HYDROGEN BOND; MOLECULAR MODEL; PRIORITY JOURNAL; QUANTUM MECHANICS; RING OPENING; SPECTROSCOPY; SYNTHESIS; VIBRATIONAL CIRCULAR DICHROISM SPECTROSCOPY; X RAY CRYSTALLOGRAPHY;

BETA-LACTAMS; CATALYSIS; CIRCULAR DICHROISM; DIMERIZATION; HYDROGEN BONDING; LIPASE; MOLECULAR CONFORMATION; QUANTUM THEORY; SOLVENTS; STEREOISOMERISM;

EID: 33748868666     PISSN: 08990042     EISSN: 1520636X     Source Type: Journal    
DOI: 10.1002/chir.20312     Document Type: Article

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