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Palladium-catalyzed addition of disulfides and diselenides to alkynes under solvent free conditions Full article

Journal Organic and Biomolecular Chemistry
ISSN: 1477-0520 , E-ISSN: 1477-0539
Output data Year: 2004, Volume: 2, Number: 3, Article number : 284, Pages count : DOI: 10.1039/b312471a
Authors Ananikov Valentine P. 1 , Beletskaya Irina P. 2
Affiliations
1 Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect 47, Moscow, 119991, Russia
2 Lomonosov Moscow State University, Chemistry Department, Vorob'evy gory, Moscow, 119899, Russia

Abstract: An efficient methodology was developed for performing palladium-catalyzed E–E (E = S, Se) bond addition to alkynes under solvent free conditions. Compared to reaction in solvent significant enhancement of reaction rate, improved efficiency and remarkable catalyst stability were observed under solvent free conditions. The addition reactions were carried out with high stereoselectivity and yields in a short reaction time.
Cite: Ananikov V.P. , Beletskaya I.P.
Palladium-catalyzed addition of disulfides and diselenides to alkynes under solvent free conditions
Organic and Biomolecular Chemistry. 2004. V.2. N3. 284 . DOI: 10.1039/b312471a WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000189146100003
Scopus: 2-s2.0-1342303394
OpenAlex: W2123846059
Citing:
DB Citing
OpenAlex 66
Scopus 69
Web of science 67
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