262846-32-2Relevant academic research and scientific papers
Synthesis of J-111,347, a novel 1β-methylcarbapenem with broad-spectrum antibacterial activity
Imamura, Hideaki,Ohtake, Norikazu,Sakuraba, Shunji,Shimizu, Aya,Yamada, Koji,Morishima, Hajime
, p. 310 - 311 (2007/10/03)
Synthesis of J-111,347 (1), a new 1β-methylcarbapenem with broad- spectrum antibacterial activity including that against methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa, was achieved via diastereoselective preparation of a side-chain thiol 3 from an optically active (R)3,4-dihydroxybutanal 4.
Discovery of novel trans-3,5-disubstituted pyrrolidinylthio-1β-methylcarbapenems
Imamura, Hideaki,Ohtake, Norikazu,Shimizu, Aya,Sato, Hiroki,Sugimoto, Yuichi,Sakuraba, Shunji,Nagano, Rie,Nakano, Masato,Abe, Shinnosuke,Suzuki-Sato, Chihiro,Nishimura, Ikuko,Kojima, Hisaki,Tsuchiya, Yoshimi,Yamada, Koji,Hashizume, Terutaka,Morishima, Hajime
, p. 1969 - 1982 (2007/10/03)
Novel trans-3,5-disubstituted pyrrolidinylthio-1β-methylcarbapenems were designed and synthesized to provide J-111,347 (1a) as the first example of an exceptionally broad-spectrum antibiotic, showing activity against methicillin-resistant Staphyloccocus aureus (MRSA) as well as Pseudomonas aeruginosa. Further derivation of 1a afforded J-111,225 (2a), J-114,870 (3a), and J-114,871 (3b), which showed improved safety profiles and retained broad-spectrum antibacterial activities. Copyright (C) 2000 Elsevier Science Ltd.
