Nickel-catalyzed and Li-mediated regiospecific C–H arylation of benzothiophenes-Reference-Cited by-同舟云学术

Nickel-catalyzed and Li-mediated regiospecific C–H arylation of benzothiophenes

Published:2020 Issue:10 Volume:22 Page:3155-3161
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Mohr Yorck¹²³⁴⁵^ORCID,Hisler Gaëlle¹²³⁴⁵,Grousset Léonie¹²³⁴⁵,Roux Yoann¹²³⁴⁵,Quadrelli Elsje Alessandra⁶²⁷³⁸,Wisser Florian M.⁹¹⁰¹¹¹²^ORCID,Canivet Jérôme¹²³⁴⁵^ORCID

Affiliation:

1. Univ. Lyon

2. Université Claude Bernard Lyon 1

3. CNRS

4. IRCELYON - UMR 5256

5. 69626 Villeurbanne

6. Université de Lyon

7. CPE Lyon

8. C2P2 - UMR 5265

9. Institute of Inorganic Chemistry

10. University of Regensburg

11. 93040 Regensburg

12. Germany

Abstract

A sustainable nickel-catalyzed direct C–H arylation of benzothiophenes, benzofuran and selenophene is reported for the first time.

Funder

Horizon 2020 Framework Programme

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/GC/D0GC00917B

Reference50 articles.

1. CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals

2. 3d Transition Metals for C–H Activation

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4. C–H bond activation enables the rapid construction and late-stage diversification of functional molecules

5. Synthesis of Extended π‐Systems through C–H Activation

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