Literature DB >> 27348581

Aerobic Oxidative Carbonylation of Enamides by Merging Palladium with Photoredox Catalysis.

Kun Liu1, Minzhu Zou1, Aiwen Lei1,2.   

Abstract

Intramolecular oxidative carbonylation reaction is an efficient approach for constructing heterocycles. However, stoichiometric amount of hypervalent metal salts is usually required in this transformation. Here we show an aerobic intramolecular oxidative carbonylation of enamides by combining palladium and photoredox catalysis. The dual catalytic system enables oxygen directly as oxidant, which provides a mild and environmentally friendly method for the synthesis of 1,3-oxazin-6-ones.

Entities:  

Year:  2016        PMID: 27348581     DOI: 10.1021/acs.joc.6b00965

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Heck Reaction of Electronically Diverse Tertiary Alkyl Halides.

Authors:  Daria Kurandina; Mónica Rivas; Maxim Radzhabov; Vladimir Gevorgyan
Journal:  Org Lett       Date:  2018-01-05       Impact factor: 6.005

2.  Visible Light-Induced Room-Temperature Heck Reaction of Functionalized Alkyl Halides with Vinyl Arenes/Heteroarenes.

Authors:  Daria Kurandina; Marvin Parasram; Vladimir Gevorgyan
Journal:  Angew Chem Int Ed Engl       Date:  2017-10-09       Impact factor: 15.336

Review 3.  When metal-catalyzed C-H functionalization meets visible-light photocatalysis.

Authors:  Lucas Guillemard; Joanna Wencel-Delord
Journal:  Beilstein J Org Chem       Date:  2020-07-21       Impact factor: 2.883

  3 in total

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