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Volumn 67, Issue 11, 2002, Pages 3953-3956
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General approach for the stereocontrolled construction of the β-lactam ring in amino acid-derived 4-alkyl-4-carboxy-2-azetidinones
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Author keywords
[No Author keywords available]
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Indexed keywords
CYCLIZATION;
AMINO ACIDS;
DERIVATIVES;
SYNTHESIS (CHEMICAL);
STEREOCHEMISTRY;
10 (N,N DICYCLOHEXYLSULFAMOYL)ISOBORNEOL;
4 CARBOXY 2 AZETIDINONE;
ACETIC ACID DERIVATIVE;
AMINO ACID DERIVATIVE;
AZETIDINONE DERIVATIVE;
BETA LACTAM;
ISOBORNEOL;
N ALPHA CHLOROACETYL;
SULFONAMIDE;
UNCLASSIFIED DRUG;
2 AZETIDINONE;
2-AZETIDINONE;
AMINO ACID;
AZETIDINE DERIVATIVE;
DIPEPTIDE;
ARTICLE;
CHEMICAL STRUCTURE;
CHIRALITY;
CYCLIZATION;
MOLECULAR INTERACTION;
REACTION ANALYSIS;
STEREOCHEMISTRY;
STRUCTURE ANALYSIS;
SYNTHESIS;
CHEMISTRY;
STEREOISOMERISM;
AMINO ACIDS;
AZETIDINES;
DIPEPTIDES;
LACTAMS;
STEREOISOMERISM;
SUPPORT, NON-U.S. GOV'T;
BETA-LACTAMS;
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EID: 0037204722
PISSN: 00223263
EISSN: None
Source Type: Journal
DOI: 10.1021/jo025571j Document Type: Article |
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Times cited : (31)
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References (46)
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