Literature DB >> 33848168

Dehydrogenative C-H Phenochalcogenazination.

Christopher Cremer1, M Alexander Eltester1, Hicham Bourakhouadar1, Iuliana L Atodiresei1, Frederic W Patureau1.   

Abstract

Heavy-atom-modified chalcogen-fused triarylamine organic materials are becoming increasingly important in the photochemical sciences. In this context, the general and direct dehydrogenative C-H phenochalcogenazination of phenols with the heavier chalcogens selenium and tellurium is herein described. The latter dehydrogenative C-N bond-forming processes operate under simple reaction conditions with highly sustainable O2 serving as the terminal oxidant.

Entities:  

Year:  2021        PMID: 33848168     DOI: 10.1021/acs.orglett.1c00573

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


  4 in total

1.  Te(II)-Catalyzed Cross-Dehydrogenative Phenothiazination of Anilines.

Authors:  Pooja Y Vemuri; Christopher Cremer; Frederic W Patureau
Journal:  Org Lett       Date:  2022-02-22       Impact factor: 6.005

2.  O2-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles.

Authors:  Christopher Cremer; Frederic W Patureau
Journal:  JACS Au       Date:  2022-06-16

3.  Effects of the Chalcogenide Identity in N-Aryl Phenochalcogenazine Photoredox Catalysts.

Authors:  Daniel A Corbin; Christopher Cremer; Katherine O Puffer; Brian S Newell; Frederic W Patureau; Garret M Miyake
Journal:  ChemCatChem       Date:  2022-07-08       Impact factor: 5.497

4.  O2-Mediated Dehydrogenative Phenoxazination of Phenols.

Authors:  Rajaa Benchouaia; Shiny Nandi; Clemens Maurer; Frederic W Patureau
Journal:  J Org Chem       Date:  2022-03-11       Impact factor: 4.354

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.