Iron-Catalyzed Coupling of Propargyl Bromides and Alkyl Grignard Reagents-Reference-Cited by-同舟云学术

Iron-Catalyzed Coupling of Propargyl Bromides and Alkyl Grignard Reagents

Published:2018-08-24 Issue:35 Volume:2018 Page:4900-4904
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Domingo-Legarda Pablo¹,Soler-Yanes Rita¹,Quirós-López M. Teresa¹,Buñuel Elena¹,Cárdenas Diego J.¹^ORCID

Affiliation:

1. Department of Organic Chemistry; Facultad de Ciencias; Universidad Autónoma de Madrid; Institute for Advanced Research in Chemical Sciences (IAdChem); Campus de Cantoblanco 28049 Madrid Spain

Funder

Secretary of State of Research, Development and Innovation

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201800849/fullpdf

Reference92 articles.

1. From Dimethylamine to Pyrrolidine: The Development of an Improved Nickel Pincer Complex for Cross-Coupling of Nonactivated Secondary Alkyl Halides

2. Nickel-catalyzed cross coupling of non-activated alkyl halides: a mechanistic perspective

3. Cross-Coupling of Nonactivated Alkyl Halides with Alkynyl Grignard Reagents: A Nickel Pincer Complex as the Catalyst

4. Cross-Coupling of Nonactivated Alkyl Halides with Alkynyl Grignard Reagents: A Nickel Pincer Complex as the Catalyst

5. Why Are (NN2)Ni Pincer Complexes Active for Alkyl−Alkyl Coupling: β-H Elimination Is Kinetically Accessible but Thermodynamically Uphill

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