Literature DB >> 19803467

Arylation of benzo-fused 1,4-quinones by the addition of boronic acids under dicationic Pd(II)-catalysis.

María Teresa Molina1, Cristina Navarro, Ana Moreno, Aurelio G Csákÿ.   

Abstract

The first examples of the direct arylation of benzo-fused 1,4-quinones by the dicationic Pd(II)-catalyzed addition of arylboronic acids are reported. The addition reaction is carried out under very mild conditions (dioxane-H(2)O, rt, open air atmosphere) and is tolerant of free OH groups. In addition, the reaction shows high regioselectivity when using nonsymmetrical quinones as starting materials.

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Year:  2009        PMID: 19803467     DOI: 10.1021/ol902084g

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


  4 in total

1.  Practical C-H functionalization of quinones with boronic acids.

Authors:  Yuta Fujiwara; Victoriano Domingo; Ian B Seiple; Ryan Gianatassio; Matthew Del Bel; Phil S Baran
Journal:  J Am Chem Soc       Date:  2011-02-22       Impact factor: 15.419

2.  Trypanosoma cruzi mitochondrial swelling and membrane potential collapse as primary evidence of the mode of action of naphthoquinone analogues.

Authors:  Kelly Salomão; Natalia A De Santana; Maria Teresa Molina; Solange L De Castro; Rubem F S Menna-Barreto
Journal:  BMC Microbiol       Date:  2013-09-03       Impact factor: 3.605

3.  Photochemical C-H Arylation of Napthoquinones Using Eosin Y.

Authors:  Bhawana Nagar; Basab Bijayi Dhar
Journal:  ACS Omega       Date:  2022-08-31

4.  Palladium-catalyzed direct C-H functionalization of benzoquinone.

Authors:  Sarah E Walker; James A Jordan-Hore; David G Johnson; Stuart A Macgregor; Ai-Lan Lee
Journal:  Angew Chem Int Ed Engl       Date:  2014-10-10       Impact factor: 15.336

  4 in total

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