STEREOCONTROLLED SYNTHESIS OF 4-ACETOXY-2-AZETIDINONE VIA DOUBLE AZETIDINONE RING FORMATION - A USEFUL PRECURSOR OF CARBAPENEM AND PENEM ANTIBIOTICS

Authors
KWON HA LEE MJ LEE IH LEE SJ YOON TH HWANG TS
Citation
Ha. Kwon et al., STEREOCONTROLLED SYNTHESIS OF 4-ACETOXY-2-AZETIDINONE VIA DOUBLE AZETIDINONE RING FORMATION - A USEFUL PRECURSOR OF CARBAPENEM AND PENEM ANTIBIOTICS, Bulletin of the Korean Chemical Society, 18(5), 1997, pp. 475-478
Citations number
20
Categorie Soggetti
Chemistry
Journal title
Bulletin of the Korean Chemical Society → ACNP
ISSN journal
02532964
Volume
18
Issue
5
Year of publication
1997
Pages
475 - 478
Database
ISI
SICI code
0253-2964(1997)18:5<475:SSO4VD>2.0.ZU;2-J
Abstract
R-tert-butyldimethylsilyloxy)ethyl]-2-azetidinone, one of the best syn thons for carbapenems and penems was efficiently synthesized from read ily available L-threonine via double azetidinone ring formation.