Articles written in Journal of Chemical Sciences
Volume 127 Issue 11 November 2015 pp 1957-1966 Articles
An efficient and a facile route to spiro-𝛽-lactams is described. 3-allyl-3-methylthio-𝛽-lactams, which are synthesized through a Lewis acid mediated C-3 alkylation of the
Volume 128 Issue 11 November 2016 pp 1745-1753 Regular Article
An effective and stereoselective synthesis of 3-(1'-methyl/phenylallyl)-3-phenylthio-β-lactams (3/4) using substituted allylsilane and Lewis acid is described. The reaction leads to the formation of a mixture of C-3 substituted allyl β-Lactams. However, these compounds on desulphurisation using tri-n-butyltinhydride and Raney Ni provide two separable diastereomers of the reduced product.
Volume 135, 2023
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