Issue 35, 2022

One-pot synthesis of α-sulfoximinophosphonate via Kabachnik–Fields reaction

Abstract

Herein, we disclose a novel approach for the synthesis of hitherto unknown α-sulfoximinophosphonate via the Kabachnik–Fields reaction of aldehyde, dialkylphosphite and sulfoximine in the presence of InCl3 in THF at 70 °C. α-Sulfoximinophosphonate is synthesized in good yields and its synthetic utilities are proved by functionalizing bromine through the Pd-catalyzed Suzuki–Miyaura cross-coupling reaction and reduction of a nitro group through the Béchamp reduction.

Graphical abstract: One-pot synthesis of α-sulfoximinophosphonate via Kabachnik–Fields reaction

Supplementary files

Article information

Article type
Communication
Submitted
26 Jul 2022
Accepted
18 Aug 2022
First published
19 Aug 2022

Org. Biomol. Chem., 2022,20, 7036-7039

One-pot synthesis of α-sulfoximinophosphonate via Kabachnik–Fields reaction

K. Natarajan, S. Sharma, C. P. Irfana Jesin, R. Kataria and G. C. Nandi, Org. Biomol. Chem., 2022, 20, 7036 DOI: 10.1039/D2OB01355J

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