Sulfinimidate Esters as an Electrophilic Sulfinimidoyl Motif Source: Synthesis of -Protected Sulfilimines from Grignard Reagents.

Org Lett

Flow Chemistry and Microreactor Technology FLAME-Lab, Department of Pharmacy - Drug Sciences, University of Bari "A. Moro", Via E. Orabona 4, Bari I-70125, Italy.

Published: September 2021

In this work we investigated, for the first time, the reactivity of sulfinimidate esters as an electrophilic sulfinimidoyl motif source. The reaction of such sulfinimidate esters with Grignard reagents enables the preparation of protected sulfilimines in high yields and with a remarkable structural variability. Moreover, the transformation can be performed in CPME (cyclopentyl methyl ether) as a green solvent under environmentally responsible conditions.

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http://dx.doi.org/10.1021/acs.orglett.1c02413DOI Listing

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