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 |
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ASJC Scopus subject areas
- Organic Chemistry
Cite this
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. / Yusybov, M. S.; Filimonov, V. D.
In: Synthesis, No. 2, 1991, p. 131-132.Research output: Contribution to journal › Article
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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 -