Literature DB >> 20016661

Chemoselective Three-Component Coupling via A Tandem Pd Catalyzed Boron-Heck and Suzuki Reaction.

Justin O'Neill1, Kyung Soo Yoo, Kyung Woon Jung.   

Abstract

Reported herein is a new approach to prepare biaryl derivatives via a tandem Pd catalyzed boron-Heck and Suzuki reaction. This one-pot tandem process avoided purification or addition of extra catalyst between steps. The resulting biaryl compounds can be prepared with substrate variability in good to moderate yields.

Entities:  

Year:  2008        PMID: 20016661      PMCID: PMC2598413          DOI: 10.1016/j.tetlet.2008.10.039

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN: 0040-4039            Impact factor:   2.415


  12 in total

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8.  Oxidative palladium(II) catalysis: A highly efficient and chemoselective cross-coupling method for carbon-carbon bond formation under base-free and nitrogenous-ligand conditions.

Authors:  Kyung Soo Yoo; Cheol Hwan Yoon; Rajesh K Mishra; Young Chun Jung; Sung Wook Yi; Kyung Woon Jung
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9.  Biphenylcarboxamide derivatives as antagonists of platelet-activating factor.

Authors:  J W Tilley; J W Clader; S Zawoiski; M Wirkus; R A LeMahieu; M O'Donnell; H Crowley; A F Welton
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10.  Toward safer methodologies for the synthesis of polyheterocyclic systems: intramolecular arylation of arenes under Mizoroki-Heck reaction conditions.

Authors:  Susana Hernández; Raul SanMartin; Imanol Tellitu; Esther Domínguez
Journal:  Org Lett       Date:  2003-04-03       Impact factor: 6.005

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  2 in total

1.  Regioselective aerobic oxidative Heck reactions with electronically unbiased alkenes: efficient access to α-alkyl vinylarenes.

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2.  Expanded substrate scope and improved reactivity of ether-forming cross-coupling reactions of organotrifluoroborates and acetals.

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  2 in total

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