Isolable and Readily Handled Halophosphonium Pre-reagents for Hydro- and Deuteriohalogenation
Author:
Affiliation:
1. Department of Chemistry, The Scripps Research Institute, 130 Scripps Way, Jupiter, Florida 33458, United States
2. Department of Chemistry, University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, United States
Funder
Belgian American Educational Foundation
University of Chicago
Scripps Research Institute
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.6b12653
Reference85 articles.
1. Solomons, T. W. G.; Fryhle, C. B.; Snyder, S. A.Organic Chemistry,12th ed.Wiley, 2016; pp1124.
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3. Nickel-Catalyzed Carbon–Carbon Bond-Forming Reactions of Unactivated Tertiary Alkyl Halides: Suzuki Arylations
4. Ni-Catalyzed Reductive Coupling of Alkyl Acids with Unactivated Tertiary Alkyl and Glycosyl Halides
5. Nickel-Catalyzed Reductive Coupling of Aryl Bromides with Tertiary Alkyl Halides
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