Nickel-catalyzed borylative coupling of alkynes, enones, and bis(pinacolato)diboron as a route to substituted alkenyl boronates

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Nickel-catalyzed borylative coupling of alkynes, enones, and bis(pinacolato)diboron as a route to substituted alkenyl boronates

Author : Dr. S. Mannathan

Year : 2009

Source Title : Angewandte Chemie - International Edition

Document Type :

Abstract

(Chemical Equation Presented) Three-component coupling reactions of an alkyne, an enone, and a diboron reagent provide access to highly substituted alkenyl boronates in good to excellent yields (see scheme). The coupling is highly regio- and stereoselective, and the products are amenable to further functional-group transformations. R1,R2=H, alkyl, aryl, CO2Me; R3=alkyl, Ph; R4,R5=H, alkyl. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.