Literature DB >> 28990038

An Ir-photoredox-catalyzed decarboxylative Michael addition of glyoxylic acid acetal as a formyl equivalent.

Sheng Zhang1, Zhoumei Tan, Haonan Zhang, Juanli Liu, Wentao Xu, Kun Xu.   

Abstract

We reported herein an iridium-photoredox-catalyzed decarboxylative conjugated addition of glyoxylic acid acetals with various Michael acceptors, including unsaturated amide, ester, aldehyde, ketone, and nitrile under irradiation. Vinyl pyridine and α-aryl styrene are also suitable substrates. The reaction offers various types of acetal products, which are of synthetic significance as protected aldehydes.

Entities:  

Year:  2017        PMID: 28990038     DOI: 10.1039/c7cc06252d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Copper(II)-Catalyzed Tandem Decarboxylative Michael/Aldol Reactions Leading to the Formation of Functionalized Cyclohexenones.

Authors:  Jeonghyo Lee; Sibin Wang; Miranda Callahan; Pavel Nagorny
Journal:  Org Lett       Date:  2018-03-21       Impact factor: 6.005

Review 2.  Recent Advances in Photoredox-Mediated Radical Conjugate Addition Reactions: An Expanding Toolkit for the Giese Reaction.

Authors:  Anastasia L Gant Kanegusuku; Jennifer L Roizen
Journal:  Angew Chem Int Ed Engl       Date:  2021-07-21       Impact factor: 16.823

3.  Blue light photoredox-catalysed acetalation of alkynyl bromides.

Authors:  Xue-Li Lyu; Shi-Sheng Huang; Hong-Jian Song; Yu-Xiu Liu; Qing-Min Wang
Journal:  RSC Adv       Date:  2019-11-06       Impact factor: 4.036

  3 in total

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