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Volumn 38, Issue 5, 2001, Pages 1031-1034
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On the mechanism and stereochemistry of the formation of β-lactam derivatives of 2, 4-disubstituted-2, 3-dihydro-benzo[1, 4]diazepines
a,c a a a b b,c |
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Author keywords
[No Author keywords available]
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Indexed keywords
1 BENZOYL 2 PHENYL 4 (4' METHOXYPHENYL)[1,4] BENZODIAZEPINE;
2 CHLORO 4 METHYL 2A (4' METHOXYPHENYL) 3,5 DIHYDROAZATETRACYCLIC[1,2 D]BENZO[1,4]DIAZEPIN 1 ONE;
2 CHLORO 4 PHENYL 2A (4' METHOXYPHENYL) 3,5 DIHYDROAZATETRACYCLIC[1,2 D]BENZO[1,4]DIAZEPIN 1 ONE;
BENZODIAZEPINE DERIVATIVE;
BETA LACTAM DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
DRUG SYNTHESIS;
ENANTIOMER;
INFRARED SPECTROSCOPY;
MELTING POINT;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
REACTION ANALYSIS;
STEREOCHEMISTRY;
STEREOISOMERISM;
X RAY DIFFRACTION;
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EID: 0034750566
PISSN: 0022152X
EISSN: None
Source Type: Journal
DOI: 10.1002/jhet.5570380503 Document Type: Article |
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Times cited : (7)
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References (11)
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