A stereoselective synthesis of a key intermediate to 1β-methylcarbapenem via aziridine ring-opening reaction

Synlett

Volumn , Issue 8, 2003, Pages 1149-1150

  Kang, Sung Ho ^a   Kim, Mihyong ^a   Ryu, Do Hyun ^a  

^a Korea Advanced Institute of Science and Technology (KAIST)   (South Korea)

Author keywords

1 methylcarbapenem; Aziridine ring opening; Iodoamidation; Stereoselective synthesis; Tandem lactam formation

Indexed keywords

1BETA METHYLCARBAPENEM DERIVATIVE; ACETAMIDE; ALCOHOL; AZETIDINONE DERIVATIVE; AZIRIDINE; TRICHLOROACETIMIDIC ACID;

AMIDATION; ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; REACTION ANALYSIS; RING OPENING; STEREOCHEMISTRY;

EID: 0037715351     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-39910     Document Type: Article

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