Literature DB >> 12227782

Phenyliodonium zwitterion as an efficient electrophile in the palladium-catalyzed suzuki-type reaction: a novel method for the synthesis of 3-aryl-4-hydroxycoumarins.

Qiang Zhu1, Jie Wu, Reza Fathi, Zhen Yang.   

Abstract

[reaction: see text] A palladium-catalyzed coupling reaction of phenyliodonium zwitterions with aryl boronic acids has been developed. The unique characteristics of the mild reaction conditions and convenient synthetic accessibility of phenyliodonium zwitterions make this method a valuable tool for generating diversified 3-aryl-4-hydroxycoumarins.

Entities:  

Year:  2002        PMID: 12227782     DOI: 10.1021/ol020159b

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


  3 in total

Review 1.  Chemistry of polyvalent iodine.

Authors:  Viktor V Zhdankin; Peter J Stang
Journal:  Chem Rev       Date:  2008-12       Impact factor: 60.622

2.  Glymes as Versatile Solvents for Chemical Reactions and Processes: from the Laboratory to Industry.

Authors:  Shaokun Tang; Hua Zhao
Journal:  RSC Adv       Date:  2014       Impact factor: 3.361

Review 3.  Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms.

Authors:  Iván Cortés; L Javier Cala; Andrea B J Bracca; Teodoro S Kaufman
Journal:  RSC Adv       Date:  2020-09-10       Impact factor: 4.036

  3 in total

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