88035-31-8Relevant articles and documents
Alkylphosphonous acid diesters, novel reagents for the oxalimide cyclization to penems
Budt,Fischer,Horlein,Kirrstetter,Lattrell
, p. 5331 - 5334 (2007/10/02)
Alkylphosphonous acid diesters MeP(OR)2 3a-b were shown to be highly effective and mild reducing reagents in the oxalimide cyclization of azetidinone-1-oxalyl-4-di or tri-thiocarbonates or 4-thioesters 1a-t forming penems 2a-t at lower temperat
AN EFFICIENT SYNTHESIS OF 2-SUBSTITUTED-THIO-6-HYDROXYETHYL-PENEM-3-CARBOXYLIC ACIDS VIA 2-THIOXOPENAMS
Leanza, W. J.,DiNinno, Frank,Muthard, David A.,Wilkening, R. R.,Wildonger, Kenneth J.,et al.
, p. 2505 - 2513 (2007/10/02)
Allyl and p-nitrobenzyl (5R,6S)-6-((R)-1-(t-butyldimethylsilyloxy)ethyl)-2-thioxopenam-3-carboxylates (19) were synthesized by base mediated cyclization of the corresponding 1-carboxylmethyl-4-phenoxy(thiocarbonyl)thio-2-azetidinones (16).The thioxopenams underwent alkylation and Michael reactions to produce 2-alkylthio- and 2-alkenylthio-penem derivatives 20 and 21.