Phenylthio radical mediated synthesis of substituted 3-vinylcyclohexanones. Interruption of the ring-opening polymerization of 1,3-dioxolan-4-yl radicals.

Ken S. Feldman; Kuok Keong Vong Antonio

doi:10.1016/S0040-4039(00)94637-9

Phenylthio radical mediated synthesis of substituted 3-vinylcyclohexanones. Interruption of the ring-opening polymerization of 1,3-dioxolan-4-yl radicals.

Ken S. Feldman
, Kuok Keong Vong Antonio

Chemistry

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

33 Scopus citations

Abstract

Substituted 3-vinylcyclohexanones result from the radical mediated combination of functionalized alkenes with a vinylcyclopropyl-1,3-dioxolane reagent.

Original language	English (US)
Pages (from-to)	823-826
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	6
DOIs	https://doi.org/10.1016/S0040-4039(00)94637-9
State	Published - 1990

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)94637-9

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@article{24153381051e473ebc671339f5b97911,

title = "Phenylthio radical mediated synthesis of substituted 3-vinylcyclohexanones. Interruption of the ring-opening polymerization of 1,3-dioxolan-4-yl radicals.",

abstract = "Substituted 3-vinylcyclohexanones result from the radical mediated combination of functionalized alkenes with a vinylcyclopropyl-1,3-dioxolane reagent.",

author = "Feldman, \{Ken S.\} and Antonio, \{Kuok Keong Vong\}",

year = "1990",

doi = "10.1016/S0040-4039(00)94637-9",

language = "English (US)",

volume = "31",

pages = "823--826",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

number = "6",

}

TY - JOUR

T1 - Phenylthio radical mediated synthesis of substituted 3-vinylcyclohexanones. Interruption of the ring-opening polymerization of 1,3-dioxolan-4-yl radicals.

AU - Feldman, Ken S.

AU - Antonio, Kuok Keong Vong

PY - 1990

Y1 - 1990

N2 - Substituted 3-vinylcyclohexanones result from the radical mediated combination of functionalized alkenes with a vinylcyclopropyl-1,3-dioxolane reagent.

AB - Substituted 3-vinylcyclohexanones result from the radical mediated combination of functionalized alkenes with a vinylcyclopropyl-1,3-dioxolane reagent.

UR - https://www.scopus.com/pages/publications/0025124363

UR - https://www.scopus.com/pages/publications/0025124363#tab=citedBy

U2 - 10.1016/S0040-4039(00)94637-9

DO - 10.1016/S0040-4039(00)94637-9

M3 - Article

AN - SCOPUS:0025124363

SN - 0040-4039

VL - 31

SP - 823

EP - 826

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 6

ER -

Phenylthio radical mediated synthesis of substituted 3-vinylcyclohexanones. Interruption of the ring-opening polymerization of 1,3-dioxolan-4-yl radicals.

Abstract

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