612546-49-3Relevant academic research and scientific papers
A stereoselective synthesis of a key intermediate to 1β-methylcarbapenem via aziridine ring-opening reaction
Kang, Sung Ho,Kim, Mihyong,Ryu, Do Hyun
, p. 1149 - 1150 (2007/10/03)
A stereocontrolled synthesis of azetidinone 3 as a key intermediate to 1β-methylcarbapenem 2 has been achieved via iodoamidation of trichloroacetimidate prepared from (Z)-olefinic allylic alcohol 6, aziridine ring-opening reaction with cyanide nucleophile and a tandem β-lactam formation.
