A cascade synthesis of S-allyl benzoylcarbamothioates via Mumm-type rearrangement
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Updated: Feb 3, 2026

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
Anjali Dahiya1, Wajid Ali, Tipu Alam
1Department of Chemistry, Indian Institute of Technology Guwahati, 781 039, Assam, India. patel@iitg.ernet.in.
Abstract:
A catalyst and solvent free synthesis of S-allyl benzoylcarbamothioates has been achieved from the in situ generated benzoylcarbonimidothioates obtained by reacting MBH alcohols with aroyl isothiocyanates. An intramolecular thia-Michael addition of the in situ generated adduct triggers a Mumm-type rearrangement leading to a stereoselective synthesis of highly functionalised S-allyl benzoylcarbamothioates.
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