Highly satisfactory alkynylation of alkenyl halides via Pd-catalyzed cross-coupling with alkynylzincs and its critical comparison with the Sonogashira alkynylation
Articolo
Data di Pubblicazione:
2003
Citazione:
Highly satisfactory alkynylation of alkenyl halides via Pd-catalyzed cross-coupling with alkynylzincs and its critical comparison with the Sonogashira alkynylation / E. Negishi, M. Quian, F. Zeng, L. Anastasia, D. Babinski. - In: ORGANIC LETTERS. - ISSN 1523-7060. - 5:10(2003 May 15), pp. 1597-1600.
Abstract:
The Pd-catalyzed alkynylation of various alkenyl halides and triflates with alkynylzincs proceeds well even with alkynyl derivatives containing electron-withdrawing groups. The reaction appears to be highly general. Noteworthy is that the corresponding Sonogashira reactions under various reported conditions are significantly less satisfactory in all cases performed in this study.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Carbon bond formation; conjugated diynes; diastereoselective synthesis; multidrug-resistance; general-synthesis; convenient route; aryl halides; palladium; efficient; organozincs
Elenco autori:
E. Negishi, M. Quian, F. Zeng, L. Anastasia, D. Babinski
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