Open Access
CC BY 4.0 · Synlett 2025; 36(19): 3237-3240
DOI: 10.1055/a-2681-2944
Letter

Synthesis of Allenyl Esters by Horner–Wadsworth–Emmons-Type Reactions of Methyl 2-[Bis(benzylthio)phosphoryl]acetate and Ketenes Using Grignard Reagents

Authors

  • Michiyasu Nakao

    1   Graduate School of Pharmaceutical Sciences, Tokushima University, Sho-machi, Tokushima Japan
  • Masakazu Tabaru

    1   Graduate School of Pharmaceutical Sciences, Tokushima University, Sho-machi, Tokushima Japan
  • Ayato Imai

    1   Graduate School of Pharmaceutical Sciences, Tokushima University, Sho-machi, Tokushima Japan
  • Syuji Kitaike

    1   Graduate School of Pharmaceutical Sciences, Tokushima University, Sho-machi, Tokushima Japan
  • Shigeki Sano

    1   Graduate School of Pharmaceutical Sciences, Tokushima University, Sho-machi, Tokushima Japan

Funding Information This work was supported by JSPS KAKENHI Grant Numbers JP20K06966 and JP23K06026.


Graphical Abstract

Abstract

Methyl 2-[bis(benzylthio)phosphoryl]acetate and its analogues have proven to be efficient Horner–Wadsworth–Emmons (HWE)-type reagents for synthesizing conjugated allenyl esters and their analogues through reactions with disubstituted ketenes using Grignard reagents. A series of HWE-type reagents containing the bis(benzylthio)phosphoryl group showed better reactivity than the corresponding HWE reagents, where two phosphorus–sulfur bonds were substituted with phosphorus–oxygen bonds.



Publication History

Received: 20 May 2025

Accepted after revision: 08 August 2025

Accepted Manuscript online:
11 August 2025

Article published online:
03 September 2025

© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).

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