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Stereo- and Regioselective Functionalization of Alkynes Catalyzed by Platinum(IV) and Palladium(II) Complexes in the System I--I3--H2O/MeOH Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1608-3393 , E-ISSN: 1070-4280
Output data Year: 2002, Volume: 38, Number: 5, Pages: 636-650 Pages count : 15 DOI: 10.1023/a:1019646619165
Authors Ananikov V.P. 1 , Mitchenko S.A. 2 , Beletskaya I.P. 3
Affiliations
1 Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia
2 Nesmeyanov Institute of Organometallic Compounds, Russian Academy of Sciences, Moscow, Russia
3 Department of Chemistry, Moscow State University, Vorob'evy gory, Moscow, 119899, Russia

Abstract: Activation of the CÍÄC bond in acetylenic hydrocarbons, catalyzed by iodide complexes of platinum(IV), and the subsequent CÄC coupling reaction make it possible to synthesize 1,4-diiodo-substituted dienes with high stereo- and regioselectivity. The reaction involves intermediate formation of bis-σ-vinyl platinum(IV) complexes which can be isolated in the pure state. Under similar conditions palladium(II) complexes catalyze iodine addition to acetylene.
Cite: Ananikov V.P. , Mitchenko S.A. , Beletskaya I.P.
Stereo- and Regioselective Functionalization of Alkynes Catalyzed by Platinum(IV) and Palladium(II) Complexes in the System I--I3--H2O/MeOH
Russian Journal of Organic Chemistry. 2002. V.38. N5. P.636-650. DOI: 10.1023/a:1019646619165 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000177753300004
Scopus: 2-s2.0-0036344289
OpenAlex: W2951894147
Citing:
DB Citing
OpenAlex 15
Scopus 19
Web of science 19
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