Bismesitylmagnesium: a thermally stable and non-nucleophilic carbon-centered base reagent for the efficient preparation of silyl enol ethers.

William J. Kerr, Allan J. B. Watson, Douglas. Hayes

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Bismesitylmagnesium has been established as an accessible, practical, convenient, and non-nucleophilic carbon-centered base reagent for efficient access to silyl enol ethers from a series of ketone substrates at readily utilizable temps.
LanguageUndefined/Unknown
Pages5049-5051
Number of pages3
JournalChemical Communications
Issue number47
DOIs
Publication statusPublished - 2007

Keywords

  • reagents
  • silyl enol ethers
  • bismesitylmagnesium

Cite this

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title = "Bismesitylmagnesium: a thermally stable and non-nucleophilic carbon-centered base reagent for the efficient preparation of silyl enol ethers.",
abstract = "Bismesitylmagnesium has been established as an accessible, practical, convenient, and non-nucleophilic carbon-centered base reagent for efficient access to silyl enol ethers from a series of ketone substrates at readily utilizable temps.",
keywords = "reagents , silyl enol ethers , bismesitylmagnesium",
author = "Kerr, {William J.} and Watson, {Allan J. B.} and Douglas. Hayes",
year = "2007",
doi = "10.1039/b711407a",
language = "Undefined/Unknown",
pages = "5049--5051",
journal = "Chemical Communications",
issn = "1359-7345",
number = "47",

}

Bismesitylmagnesium: a thermally stable and non-nucleophilic carbon-centered base reagent for the efficient preparation of silyl enol ethers. / Kerr, William J.; Watson, Allan J. B.; Hayes, Douglas.

In: Chemical Communications, No. 47, 2007, p. 5049-5051.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Bismesitylmagnesium: a thermally stable and non-nucleophilic carbon-centered base reagent for the efficient preparation of silyl enol ethers.

AU - Kerr, William J.

AU - Watson, Allan J. B.

AU - Hayes, Douglas.

PY - 2007

Y1 - 2007

N2 - Bismesitylmagnesium has been established as an accessible, practical, convenient, and non-nucleophilic carbon-centered base reagent for efficient access to silyl enol ethers from a series of ketone substrates at readily utilizable temps.

AB - Bismesitylmagnesium has been established as an accessible, practical, convenient, and non-nucleophilic carbon-centered base reagent for efficient access to silyl enol ethers from a series of ketone substrates at readily utilizable temps.

KW - reagents

KW - silyl enol ethers

KW - bismesitylmagnesium

U2 - 10.1039/b711407a

DO - 10.1039/b711407a

M3 - Article

SP - 5049

EP - 5051

JO - Chemical Communications

T2 - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

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