(Q29307870)

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Palladium Round Trip in the Negishi Coupling of trans-[PdMeCl(PMePh2)2] with ZnMeCl: An Experimental and DFT Study of the Transmetalation Step

scientific article (publication date: 7 July 2010)

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Palladium Round Trip in the Negishi Coupling of trans-[PdMeCl(PMePh2)2] with ZnMeCl: An Experimental and DFT Study of the Transmetalation Step (English)

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

Max García-Melchor

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Max García-Melchor

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Gregori Ujaque

6

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Feliu Maseras

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Pablo Espinet

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Agustí Lledós

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Agustí Lledós

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Beatriz Fuentes

1

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

Juan A. Casares

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

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publication date

7 July 2010

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

Chemistry—A European Journal

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

16

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

29

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

8596-8599

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https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

Palladium-catalyzed negishi cross-coupling reactions of unactivated alkyl iodides, bromides, chlorides, and tosylates

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201001332

21 January 2018

Analysis of key steps in the catalytic cross-coupling of alkyl electrophiles under Negishi-like conditions

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201001332

21 January 2018

Insights into the mechanism of the Negishi reaction: ZnRX versus ZnR2 reagents

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201001332

21 January 2018

Revealing a second transmetalation step in the Negishi coupling and its competition with reductive elimination: improvement in the interpretation of the mechanism of biaryl syntheses.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201001332

21 January 2018

Mechanisms of 1,1-reductive elimination from palladium

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201001332

21 January 2018

Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3Catalyzed bytrans-[PdR1IL2] (R1= C6Cl2F3; R2= Vinyl, 4-Methoxyphenyl; L = AsPh3)

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201001332

21 January 2018

Mechanism of the Stille Reaction. 2. Couplings of Aryl Triflates with Vinyltributyltin. Observation of Intermediates. A More Comprehensive Scheme

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201001332

21 January 2018

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10.1002/CHEM.201001332

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DOI.org query endpoint

https://doi.org/10.1002%2FCHEM.201001332

9 April 2017

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