Low-cost transition metal catalysed Negishi coupling: an update-Reference-Cited by-同舟云学术

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Low-cost transition metal catalysed Negishi coupling: an update

Published:2023 Issue:32 Volume:21 Page:6438-6455
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Rinu Pulluparambil Xavier Thresia¹,Philip Rose Mary¹,Anilkumar Gopinathan¹^ORCID

Affiliation:

1. School of Chemical Sciences, Mahatma Gandhi University, Priyadarsini Hills P O, Kottayam, Kerala, 686560 India

Abstract

This review highlights the recent strategies and potential of low-cost transition metal (Fe, Co, Ni and Cu) catalysed Negishi coupling reactions.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00784G

Reference58 articles.

1. Activation of Grignard reagents by transition-metal complexes. A new and simple synthesis of trans-stilbenes and polyphenyls

2. Selective carbon-carbon bond formation by cross-coupling of Grignard reagents with organic halides. Catalysis by nickel-phosphine complexes

3. Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides

4. Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides

5. A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium

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