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.

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.

Highly satisfactory alkynylation of alkenyl halides via Pd-catalyzed cross-coupling with alkynylzincs and its critical comparison with the Sonogashira alkynylation

L. Anastasia
Penultimo
;
2003

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.
Carbon bond formation; conjugated diynes; diastereoselective synthesis; multidrug-resistance; general-synthesis; convenient route; aryl halides; palladium; efficient; organozincs
Settore BIO/10 - Biochimica
15-mag-2003
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/37775
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