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Photocatalytic decarboxylation of free carboxylic acids and their functionalization.
Mondal, Subal; Mandal, Subham; Mondal, Soumya; Midya, Siba P; Ghosh, Pradyut.
Afiliação
  • Mondal S; School of Chemical Sciences, Indian Association for the Cultivation of Science, Kolkata 700032, India. icpg@iacs.res.in.
  • Mandal S; School of Chemical Sciences, Indian Association for the Cultivation of Science, Kolkata 700032, India. icpg@iacs.res.in.
  • Mondal S; School of Chemical Sciences, Indian Association for the Cultivation of Science, Kolkata 700032, India. icpg@iacs.res.in.
  • Midya SP; Department of Chemistry, Jadavpur University, 188 Raja S. C. Mullick Road, Kolkata 700032, India.
  • Ghosh P; School of Chemical Sciences, Indian Association for the Cultivation of Science, Kolkata 700032, India. icpg@iacs.res.in.
Chem Commun (Camb) ; 2024 Aug 09.
Article em En | MEDLINE | ID: mdl-39120531
ABSTRACT
Visible light mediated decarboxylative functionalization of carboxylic acids and their derivatives has recently emerged as a novel and powerful toolkit for small molecule activation in diverse carbon-carbon and carbon-hetero bond forming reactions. Naturally abundant highly functionalized bench-stable carboxylic acid analogs have been employed as promising alternatives to non-trivial organometallic reagents for mild and eco-benign synthetic transformation with traceless CO2 by-products. In this highlight article, we focus on the development of various photodecarboxylative functionalization strategies along with intra/inter-molecular cyclization via concerted single electron transfer (SET) or energy transfer (ET) pathways. Moreover, widely explored carboxylic acids are systematically classified here into four categories; i.e., α-keto, aliphatic, α,ß-unsaturated, and aromatic analogs for a concise overview to the readership. The association of decarboxylative radical species with coupling partners to construct C-C and C-N/O/S/P/X bonds for each analogous acid has been presented in brief.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article