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

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

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

Original languageEnglish (US)
Pages (from-to)823-826
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number6
DOIs
StatePublished - Jan 1 1990

Fingerprint

Ring opening polymerization
Alkenes
Polymerization
formal glycol

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

@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",
month = "1",
day = "1",
doi = "10.1016/S0040-4039(00)94637-9",
language = "English (US)",
volume = "31",
pages = "823--826",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "6",

}

Phenylthio radical mediated synthesis of substituted 3-vinylcyclohexanones. Interruption of the ring-opening polymerization of 1,3-dioxolan-4-yl radicals. / Feldman, Ken S.; Antonio, Kuok Keong Vong.

In: Tetrahedron Letters, Vol. 31, No. 6, 01.01.1990, p. 823-826.

Research output: Contribution to journalArticle

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 - 1990/1/1

Y1 - 1990/1/1

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 - http://www.scopus.com/inward/record.url?scp=0025124363&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025124363&partnerID=8YFLogxK

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

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

M3 - Article

VL - 31

SP - 823

EP - 826

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 6

ER -