Ester-directed Ru-catalyzed C-O activation/C-C coupling reaction of ortho-methoxy naphthoates with organoboroneopentylates.

Chem Commun (Camb)

Department of Chemistry, Queen's University, 90 Bader Lane, Kingston, K7L 3N6, Ontario, Canada.

Published: January 2016

A new, catalytic and general synthetic methodology for the construction of biaryls and heterobiaryls by the cross-coupling of ortho-methoxy naphthoates with organoboroneopentylates is disclosed. The reaction proceeds under RuH2(CO)(PPh3)3-catalyzed conditions driven by unreactive C-O bond activation of a proximate ester directing group (DG)-catalyst chelation. This one-step synthesis of 2-aryl and -heteroaryl-1-naphthoates has the features of operational simplicity, minimum waste and convenient scale-up. The hierarchy of C(O)Me > CONEt2 > CO2Me coordination-assisted reactivity, of potential value in chemoselective synthesis, is also established.

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http://dx.doi.org/10.1039/c5cc09121gDOI Listing

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Ester-directed Ru-catalyzed C-O activation/C-C coupling reaction of ortho-methoxy naphthoates with organoboroneopentylates.

Chem Commun (Camb)

January 2016

Department of Chemistry, Queen's University, 90 Bader Lane, Kingston, K7L 3N6, Ontario, Canada.

A new, catalytic and general synthetic methodology for the construction of biaryls and heterobiaryls by the cross-coupling of ortho-methoxy naphthoates with organoboroneopentylates is disclosed. The reaction proceeds under RuH2(CO)(PPh3)3-catalyzed conditions driven by unreactive C-O bond activation of a proximate ester directing group (DG)-catalyst chelation. This one-step synthesis of 2-aryl and -heteroaryl-1-naphthoates has the features of operational simplicity, minimum waste and convenient scale-up.

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