A novel, mild, and facile method to prepare 6-methylidene pe nem derivatives

Journal of Organic Chemistry

Volumn 69, Issue 18, 2004, Pages 5850-5860

  Abe, Takao ^a,d   Sato, Chisato ^a   Ushirogochi, Hideki ^a   Sato, Koichi ^a   Takasaki, Tsuyoshi ^a   Isoda, Takeshi ^a   Mihira, Ado ^a   Yamamura, Itsuki ^a   Hayashi, Kazuhiko ^a   Kumagai, Toshio ^a   Tamai, Satoshi ^a   Shiro, Motoo ^b   Venkatesan, Aranapakam M ^c   Mansour, Tarek S ^c  

^a Wyeth Lederle Japan Ltd   (Japan)

^b RIGAKU CORPORATION   (Japan)

^c WYETH RESEARCH   (United States)

^d MEIJI SEIKA KAISHA LTD   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BROMOHYDRIN; PENEM;

ACETYLATION; ALCOHOLS; CONDENSATION; MAGNESIUM COMPOUNDS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

OLEFINS;

4 NITROBENZYL 6 BROMO 7 OXO 4 THIA 1 AZABICYCLO[3.2.0]HEPT 2 ENE 2 CARBOXYLATE; 6 (1 METHYL 1,2,3 TRIAZOL 4 YLMETHYLENE)PENEM 3 CARBOXYLIC ACID; 6 METHYLIDENE PENEM DERIVATIVE; ASPARENOMYCIN A; ASPARENOMYCIN B; ASPARENOMYCIN C; BETA LACTAMASE INHIBITOR; CARBAPENEM DERIVATIVE; PENEM DERIVATIVE; SB 206999Z; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CHEMICAL STRUCTURE; ENZYME INHIBITION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

CATALYSIS; CHEMISTRY, ORGANIC; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; LACTAMS; MOLECULAR STRUCTURE; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 4344693782     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo049880g     Document Type: Article

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