Solvent-free palladium-catalyzed addition of diaryl dichalcogenides to alkynes

Solvent-free palladium-catalyzed addition of diaryl dichalcogenides to alkynes Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2004, Volume: 53, Number: 3, Pages: 561-565 Pages count : 5 DOI: 10.1023/b:rucb.0000035637.57608.51

Authors

Ananikov V.P. ¹ , Beletskaya I.P. ²

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
2	Department of Chemistry, M. V. Lomonosov Moscow State University, Leninskie Gory, 119992 Moscow, Russian Federation

Solvent-free palladium-catalyzed addition of diaryl disulfides and diselenides to terminal alkynes makes it possible to achieve high stereoselectivity and almost 100% yields in ≈10 min using only 0.1 mol.% catalyst. Both Pd(PPh3)4 and easily available Pd(OAc)2 and PdCl2 can be used in the reaction with an excess of triphenylphosphine. The catalyst and triphenylphosphine are readily recycled for repeated use. The study of the mechanism of the solvent-free catalytic reaction indicates that the process involves binuclear palladium complexes.

Ananikov V.P. , Beletskaya I.P.
Solvent-free palladium-catalyzed addition of diaryl dichalcogenides to alkynes
Russian Chemical Bulletin. 2004. V.53. N3. P.561-565. DOI: 10.1023/b:rucb.0000035637.57608.51 Scopus OpenAlex

Scopus:	2-s2.0-4043167764
OpenAlex:	W2950079142

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OpenAlex	18
Scopus	19