115459-76-2Relevant academic research and scientific papers
RETENTION OF STEREOCHEMISTRY IN THE RING-OPENING OF PENICILLIN V SULPHONE p-NITROBENZYL ESTER
Davis, Michael,Wu, Wen-Yang
, p. 183 - 188 (2007/10/02)
By careful control of the basic catalyst, the solvent, and the temperature, p-nitrobenzyl phenoxymethylpenicillinate 1,1-dioxide (penicillin V sulphone p-nitrobenzyl ester) (1d) can be converted into (2R,3R)-1-2-methyl-(p-nitrobenzyloxycarbonyl)prop-1-en
