Literature DB >> 25689275

Cobalt-promoted dimerization of aminoquinoline benzamides.

Liene Grigorjeva1, Olafs Daugulis.   

Abstract

A method for aminoquinoline-directed, cobalt-promoted dimerization of benzamides has been developed. Reactions proceed in ethanol solvent in the presence of Mn(OAc)2 cocatalyst and Na2CO3 base and use oxygen as a terminal oxidant. Bromo, iodo, nitro, ether, and ester moieties are compatible with the reaction conditions. Cross-coupling of electronically dissimilar aminoquinoline benzamides proceeds with modest yields and selectivities.

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Year:  2015        PMID: 25689275      PMCID: PMC4352950          DOI: 10.1021/acs.orglett.5b00155

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  57 in total

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10.  Copper(II)-mediated dehydrogenative cross-coupling of heteroarenes.

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  8 in total

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4.  Cobalt-Catalyzed, Aminoquinoline-Directed Functionalization of Phosphinic Amide sp2 C-H Bonds.

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6.  Co-catalyzed ortho-C-H functionalization/annulation of arenes and alkenes with alkynylsilanes: access to isoquinolone and pyridone motifs.

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7.  Insights into Cobalta(III/IV/II)-Electrocatalysis: Oxidation-Induced Reductive Elimination for Twofold C-H Activation.

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8.  Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.

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  8 in total

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