Intramolecular anodic olefin coupling reactions: the use of allylsilanes

Kevin D. Moeller; Christine M. Hudson

doi:10.1016/S0040-4039(00)79910-2

Intramolecular anodic olefin coupling reactions: the use of allylsilanes

Kevin D. Moeller, Christine M. Hudson

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Abstract

The use of allylsilanes as directing groups in the intramolecular electrochemical coupling of electron rich olefins has been examined. The allylsilanes were shown to provide an effective means for controlling product selectivity, and led to the formation of five- and six-membered ring products in 59-84% isolated yields.

Original language	English
Pages (from-to)	2307-2310
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	21
DOIs	https://doi.org/10.1016/S0040-4039(00)79910-2
State	Published - May 20 1991

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title = "Intramolecular anodic olefin coupling reactions: the use of allylsilanes",

abstract = "The use of allylsilanes as directing groups in the intramolecular electrochemical coupling of electron rich olefins has been examined. The allylsilanes were shown to provide an effective means for controlling product selectivity, and led to the formation of five- and six-membered ring products in 59-84% isolated yields.",

author = "Moeller, {Kevin D.} and Hudson, {Christine M.}",

note = "Funding Information: Research Fund, administered by the American Funding Information: Facility, partially supported by NIH Funding Information: work was supported by Washington University. the donors of the Petroleum",

year = "1991",

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doi = "10.1016/S0040-4039(00)79910-2",

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T2 - the use of allylsilanes

AU - Moeller, Kevin D.

AU - Hudson, Christine M.

N1 - Funding Information: Research Fund, administered by the American Funding Information: Facility, partially supported by NIH Funding Information: work was supported by Washington University. the donors of the Petroleum

PY - 1991/5/20

Y1 - 1991/5/20

N2 - The use of allylsilanes as directing groups in the intramolecular electrochemical coupling of electron rich olefins has been examined. The allylsilanes were shown to provide an effective means for controlling product selectivity, and led to the formation of five- and six-membered ring products in 59-84% isolated yields.

AB - The use of allylsilanes as directing groups in the intramolecular electrochemical coupling of electron rich olefins has been examined. The allylsilanes were shown to provide an effective means for controlling product selectivity, and led to the formation of five- and six-membered ring products in 59-84% isolated yields.

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U2 - 10.1016/S0040-4039(00)79910-2

DO - 10.1016/S0040-4039(00)79910-2

M3 - Article

AN - SCOPUS:0025728154

SN - 0040-4039

VL - 32

SP - 2307

EP - 2310

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 21

ER -

Intramolecular anodic olefin coupling reactions: the use of allylsilanes

Abstract

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