A Boron–Boron Double Transborylation Strategy for the Synthesis of gem-Diborylalkanes
Author:
Affiliation:
1. EaStCHEM School of Chemistry, University of Edinburgh, Joseph Black Building, David Brewster Road, Edinburgh EH9 3FJ, United Kingdom
2. GSK Medicines Research Centre, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, United Kingdom
Funder
Engineering and Physical Sciences Research Council
Royal Society
GlaxoSmithKline
Publisher
American Chemical Society (ACS)
Subject
Catalysis,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acscatal.0c00869
Reference79 articles.
1. Communications - Selective Conversion of Olefins into Organoboranes Through Competitive Hydroboration, Isomerization and Displacement Reactions
2. Communications - Hydroboration of Olefins. A Remakably Fast Room-Temperature Addition of Diborane to Olefins
3. Hydroboration. II. A Remarkably Fast Addition of Diborane to Olefins—Scope and Stoichiometry of the Reaction
4. Hydroboration—a powerful synthetic tool
5. Hydroboration. XVI. The Hydroboration of Olefins, Acetylenes and Dienes with Thexylborane
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