66872-16-0Relevant academic research and scientific papers
Chemistry of Cephems: C-4 Substitution and Sulphoxide De-oxygenation Reactions.
Bremner, David H.,Ringan, Neil S.
, p. 1265 - 1272 (2007/10/02)
The anion derived from ceph-3-em esters adds readily to Michael acceptors to give C-4 disubstituted ceph-2-ems.Oxidation of a typical adduct, such as the 4-cyanoethyl-4-diphenylmethyl ester, followed by ester hydrolysis and decarboxylation, gives the 4-cyanoethylceph-3-em sulphoxide which is easily reduced to the sulphide.Furthermore, zinc-acetic acid in DMF (dimethylformamide) is found to be an effective, mild reagent for the de-oxygenation of ceph-2-em sulphoxides.
The Reaction of Metal Fluorides with unsym-Azetidinone Disulfides and 2β-(Halomethyl)penams. The 3β-Fluoro-3α-methylcephams
Micetich, Ronald G.,Betageri, Sucheta,Singh, Rajeshwar,Payne, Pamela
, p. 915 - 918 (2007/10/02)
Fluorination studies on unsym-azetidinone disulfides and 2β-penams with metal fluorides are described.The unsym-azetidinone disulfides with AgF, in CH2Cl2, produce the 3β-fluoro-3α-methylcephams in low yields.The reaction of the 2
