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Iron-Catalyzed Cross-Coupling of Alkynyl and Styrenyl Chlorides with Alkyl Grignard Reagents in Batch and Flow.


ABSTRACT: Transition-metal-catalyzed cross-coupling chemistry can be regarded as one of the most powerful protocols to construct carbon-carbon bonds. While the field is still dominated by palladium catalysis, there is an increasing interest to develop protocols that utilize cheaper and more sustainable metal sources. Herein, we report a selective, practical, and fast iron-based cross-coupling reaction that enables the formation of Csp-Csp3 and Csp2 -Csp3 bonds. In a telescoped flow process, the reaction can be combined with the Grignard reagent synthesis. Moreover, flow allows the use of a supporting ligand to be avoided without eroding the reaction selectivity.

SUBMITTER: Deng Y 

PROVIDER: S-EPMC6900226 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Iron-Catalyzed Cross-Coupling of Alkynyl and Styrenyl Chlorides with Alkyl Grignard Reagents in Batch and Flow.

Deng Yuchao Y   Wei Xiao-Jing XJ   Wang Xiao X   Sun Yuhan Y   Noël Timothy T  

Chemistry (Weinheim an der Bergstrasse, Germany) 20191022 64


Transition-metal-catalyzed cross-coupling chemistry can be regarded as one of the most powerful protocols to construct carbon-carbon bonds. While the field is still dominated by palladium catalysis, there is an increasing interest to develop protocols that utilize cheaper and more sustainable metal sources. Herein, we report a selective, practical, and fast iron-based cross-coupling reaction that enables the formation of Csp-Csp<sup>3</sup> and Csp<sup>2</sup> -Csp<sup>3</sup> bonds. In a telesc  ...[more]

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