Iodine in dimethyl sulfoxide as a new general reagent for the preparative oxidation of 1,2-diarylethenes and 1,2-diarylethynes to aromatic 1,2-diketones

M. S. Yusybov, V. D. Filimonov

Research output: Contribution to journalArticle

44 Citations (Scopus)

Abstract

1,2-Diarylethenes and 1,2-diarylethynes are readily converted to the corresponding 1,2-diketones in high yield using the reagent iodine in dimethyl sulfoxide. Alkynes in these reactions are more reactive than alkenes.

Original languageEnglish
Pages (from-to)131-132
Number of pages2
JournalSynthesis
Issue number2
Publication statusPublished - 1991

Fingerprint

Alkynes
Dimethyl sulfoxide
Alkenes
Dimethyl Sulfoxide
Iodine
Olefins
Oxidation

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

@article{1d6d108b45584a7aaf82951321fcbf1e,
title = "Iodine in dimethyl sulfoxide as a new general reagent for the preparative oxidation of 1,2-diarylethenes and 1,2-diarylethynes to aromatic 1,2-diketones",
abstract = "1,2-Diarylethenes and 1,2-diarylethynes are readily converted to the corresponding 1,2-diketones in high yield using the reagent iodine in dimethyl sulfoxide. Alkynes in these reactions are more reactive than alkenes.",
author = "Yusybov, {M. S.} and Filimonov, {V. D.}",
year = "1991",
language = "English",
pages = "131--132",
journal = "Synthesis",
issn = "0039-7881",
publisher = "Georg Thieme Verlag",
number = "2",

}

TY - JOUR

T1 - Iodine in dimethyl sulfoxide as a new general reagent for the preparative oxidation of 1,2-diarylethenes and 1,2-diarylethynes to aromatic 1,2-diketones

AU - Yusybov, M. S.

AU - Filimonov, V. D.

PY - 1991

Y1 - 1991

N2 - 1,2-Diarylethenes and 1,2-diarylethynes are readily converted to the corresponding 1,2-diketones in high yield using the reagent iodine in dimethyl sulfoxide. Alkynes in these reactions are more reactive than alkenes.

AB - 1,2-Diarylethenes and 1,2-diarylethynes are readily converted to the corresponding 1,2-diketones in high yield using the reagent iodine in dimethyl sulfoxide. Alkynes in these reactions are more reactive than alkenes.

UR - http://www.scopus.com/inward/record.url?scp=0025964315&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025964315&partnerID=8YFLogxK

M3 - Article

SP - 131

EP - 132

JO - Synthesis

JF - Synthesis

SN - 0039-7881

IS - 2

ER -