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

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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 language	English
Pages (from-to)	131-132
Number of pages	2
Journal	Synthesis
Issue number	2
Publication status	Published - 1991

ASJC Scopus subject areas

Organic Chemistry

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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",

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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.

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M3 - Article

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SP - 131

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JO - Synthesis

JF - Synthesis

SN - 0039-7881

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ER -

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

ASJC Scopus subject areas

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