Issue 0, 1982

Silyl phosphites. Part 20. A facile synthesis of phosphoenolpyruvate and its analogue utilizing in situ generated trimethylsilyl bromide

Abstract

Phosphoenolpyruvate (PEP) has been synthesized from pyruvic acid and dimethyl trimethylsilyl phosphite in high yield by a new route which involves, successively, trimethylsilylation, bromination, and a Perkow reaction. A PEP analogue of 1-(dihydroxyphosphinyl)vinyl phosphate (1) has also been prepared.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 2509-2513

Silyl phosphites. Part 20. A facile synthesis of phosphoenolpyruvate and its analogue utilizing in situ generated trimethylsilyl bromide

M. Sekine, T. Futatsugi, K. Yamada and T. Hata, J. Chem. Soc., Perkin Trans. 1, 1982, 2509 DOI: 10.1039/P19820002509

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