Tunable and Practical Homogeneous Organic Reductants for Cross-Electrophile Coupling-Reference-Cited by-同舟云学术

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Tunable and Practical Homogeneous Organic Reductants for Cross-Electrophile Coupling

Published:2021-11-30 Issue:49 Volume:143 Page:21024-21036
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Charboneau David J.¹,Huang Haotian¹,Barth Emily L.¹,Germe Cameron C.¹,Hazari Nilay¹^ORCID,Mercado Brandon Q.¹,Uehling Mycah R.²,Zultanski Susan L.³

Affiliation:

1. Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States

2. Discovery Chemistry, HTE and Lead Discovery Capabilities, Merck & Co., Inc., Kenilworth, New Jersey 07033, United States

3. Department of Process Research and Development, Merck & Co., Inc., Kenilworth, New Jersey 07033, United States

Funder

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.1c10932

Reference135 articles.

1. Practical olefin hydroamination with nitroarenes

2. Catalytic Reductive Vinylidene Transfer Reactions

3. Nickel-Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms

4. Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides

5. Iron–Nickel Dual-Catalysis: A New Engine for Olefin Functionalization and the Formation of Quaternary Centers

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1. Zinc and manganese redox potentials in organic solvents and their influence on nickel-catalysed cross-electrophile coupling;Nature Chemistry;2024-09-06

2. Molecular Editing of Toluene by Sequential meta-C–H/Benzylic C–N Deaminative Functionalizations;Organic Letters;2024-08-23

3. Formate-Mediated Reductive Cross-Coupling of Vinyl Halides and Aryl Iodides: cine-Substitution via Palladium(I) Catalysis;Organic Letters;2024-08-12

4. Homogeneous organic reductant based on 4,4′- Bu2-2,2′-bipyridine for cross-electrophile coupling;Tetrahedron Letters;2024-07

5. Bis(pinacolato)diboron‐Enabled Ni‐Catalyzed Reductive Arylation/Vinylation of Alkyl Electrophiles;Advanced Science;2024-06-17

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