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Volumn 60, Issue 4, 2004, Pages 867-870
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A highly diastereoselective synthesis of a 1-β-methylcarbapenem intermediate using titanium enolate of 2′-hydroxypropiophenone
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Author keywords
Azetidinones; Carbapenems; Condensation; Enolates; Ozonolysis; Stereoselective
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Indexed keywords
2' HYDROXYPROPIOPHENONE;
4 ACETOXY BETA LACTAM;
BETA LACTAM DERIVATIVE;
CARBAPENEM DERIVATIVE;
CARBOXYLIC ACID;
KETONE;
PAROXYPROPIONE;
TITANIUM DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
OZONOLYSIS;
POLYMERIZATION;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
STEREOCHEMISTRY;
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EID: 0348230606
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2003.11.048 Document Type: Article |
Times cited : (10)
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References (16)
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