Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine Full article
Journal |
Australian Journal of Chemistry
ISSN: 0004-9425 , E-ISSN: 1445-0038 |
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Output data | Year: 2017, Volume: 70, Number: 4, Pages: 421-429 Pages count : 9 DOI: 10.1071/CH17026 | ||||||
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Abstract:
Reaction of 1,2-diaminioethane (ethylenediamine) with electron-deficient alkynes leads to full scission of the C C bond even in the absence of a keto group directly attached to the alkyne. This process involves oxidation of one of the alkyne carbons into C2 of a 2-R-4,5-dihydroimidazole with the concomitant reduction of the other carbon to a methyl group. The sequence of Sonogashira coupling with the ethylenediamine-mediated fragmentation described in this work can be used for selective formal substitution of halogen in aryl halides by a methyl group or a 4,5-dihydroimidazol-2-yl moiety.
Cite:
Vasilevsky S.F.
, Davydova M.P.
, Mamatyuk V.I.
, Tsvetkov N.
, Hughes A.
, Baranov D.S.
, Alabugin I.V.
Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
Australian Journal of Chemistry. 2017. V.70. N4. P.421-429. DOI: 10.1071/CH17026 WOS Scopus
Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
Australian Journal of Chemistry. 2017. V.70. N4. P.421-429. DOI: 10.1071/CH17026 WOS Scopus
Identifiers:
Web of science | WOS:000398533900010 |
Scopus | 2-s2.0-85016809022 |
OpenAlex | W2592711852 |