Methyltriphenoxyphosphonium trifluoromethanesulphonate: A new, versatile synthetic reagent

Edward S. Lewis; Brian J. Walker; Lucy M. Ziurys

doi:10.1039/C39780000424

Methyltriphenoxyphosphonium trifluoromethanesulphonate: A new, versatile synthetic reagent

Edward S. Lewis, Brian J. Walker, Lucy M. Ziurys

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

Methyltriphenoxyphosphonium trifluoromethanesulphonate is used to synthesise a variety of compound types including ethers, esters, nitriles, and diols and in a novel reduction of alkenes to alkanes.

Original language	English (US)
Pages (from-to)	424-425
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	10
DOIs	https://doi.org/10.1039/C39780000424
State	Published - 1978
Externally published	Yes

ASJC Scopus subject areas

Molecular Medicine

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title = "Methyltriphenoxyphosphonium trifluoromethanesulphonate: A new, versatile synthetic reagent",

abstract = "Methyltriphenoxyphosphonium trifluoromethanesulphonate is used to synthesise a variety of compound types including ethers, esters, nitriles, and diols and in a novel reduction of alkenes to alkanes.",

author = "Lewis, {Edward S.} and Walker, {Brian J.} and Ziurys, {Lucy M.}",

year = "1978",

doi = "10.1039/C39780000424",

language = "English (US)",

pages = "424--425",

journal = "Journal of the Chemical Society, Chemical Communications",

issn = "0022-4936",

publisher = "Royal Society of Chemistry",

number = "10",

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T1 - Methyltriphenoxyphosphonium trifluoromethanesulphonate

T2 - A new, versatile synthetic reagent

AU - Lewis, Edward S.

AU - Walker, Brian J.

AU - Ziurys, Lucy M.

PY - 1978

Y1 - 1978

N2 - Methyltriphenoxyphosphonium trifluoromethanesulphonate is used to synthesise a variety of compound types including ethers, esters, nitriles, and diols and in a novel reduction of alkenes to alkanes.

AB - Methyltriphenoxyphosphonium trifluoromethanesulphonate is used to synthesise a variety of compound types including ethers, esters, nitriles, and diols and in a novel reduction of alkenes to alkanes.

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U2 - 10.1039/C39780000424

DO - 10.1039/C39780000424

M3 - Article

AN - SCOPUS:37049100635

SN - 0022-4936

SP - 424

EP - 425

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 10

ER -

Methyltriphenoxyphosphonium trifluoromethanesulphonate: A new, versatile synthetic reagent

Abstract

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