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Calcium carbide as a convenient acetylene source in the synthesis of unsaturated sulfides, promising functionalized monomers. / Rodygin, Konstantin S.; Kostin, Anton A.; Ananikov, Valentine P.

In: Mendeleev Communications , Vol. 25, No. 6, 01.11.2015, p. 415-416.

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Rodygin, Konstantin S. ; Kostin, Anton A. ; Ananikov, Valentine P. / Calcium carbide as a convenient acetylene source in the synthesis of unsaturated sulfides, promising functionalized monomers. In: Mendeleev Communications . 2015 ; Vol. 25, No. 6. pp. 415-416.

BibTeX

@article{ec2a45a0584b4b1bad5016a6f22b0752,
title = "Calcium carbide as a convenient acetylene source in the synthesis of unsaturated sulfides, promising functionalized monomers",
abstract = "Calcium carbide was studied as a useful solid-state reagent to incorporate acetylene unit into synthetic procedures. Atom-economic thiol-yne click reaction was successfully performed with single and double additions. Heterocyclic thiols and aliphatic dithiols reacted with acetylene generated in situ from calcium carbide to afford corresponding vinyl sulfides and bis(thiovinyl)ethers in good to high yields.",
author = "Rodygin, {Konstantin S.} and Kostin, {Anton A.} and Ananikov, {Valentine P.}",
note = "Publisher Copyright: {\textcopyright} 2015 Mendeleev Communications. Published by ELSEVIER B.V. on behalf of the N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences.",
year = "2015",
month = nov,
day = "1",
doi = "10.1016/j.mencom.2015.11.004",
language = "English",
volume = "25",
pages = "415--416",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "6",

}

RIS

TY - JOUR

T1 - Calcium carbide as a convenient acetylene source in the synthesis of unsaturated sulfides, promising functionalized monomers

AU - Rodygin, Konstantin S.

AU - Kostin, Anton A.

AU - Ananikov, Valentine P.

N1 - Publisher Copyright: © 2015 Mendeleev Communications. Published by ELSEVIER B.V. on behalf of the N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences.

PY - 2015/11/1

Y1 - 2015/11/1

N2 - Calcium carbide was studied as a useful solid-state reagent to incorporate acetylene unit into synthetic procedures. Atom-economic thiol-yne click reaction was successfully performed with single and double additions. Heterocyclic thiols and aliphatic dithiols reacted with acetylene generated in situ from calcium carbide to afford corresponding vinyl sulfides and bis(thiovinyl)ethers in good to high yields.

AB - Calcium carbide was studied as a useful solid-state reagent to incorporate acetylene unit into synthetic procedures. Atom-economic thiol-yne click reaction was successfully performed with single and double additions. Heterocyclic thiols and aliphatic dithiols reacted with acetylene generated in situ from calcium carbide to afford corresponding vinyl sulfides and bis(thiovinyl)ethers in good to high yields.

UR - http://www.scopus.com/inward/record.url?scp=84951284731&partnerID=8YFLogxK

U2 - 10.1016/j.mencom.2015.11.004

DO - 10.1016/j.mencom.2015.11.004

M3 - Article

AN - SCOPUS:84951284731

VL - 25

SP - 415

EP - 416

JO - Mendeleev Communications

JF - Mendeleev Communications

SN - 0959-9436

IS - 6

ER -

ID: 100855145