The Matteson Reaction
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471264180.or105.03
Reference340 articles.
1. Neighboring Boron in Nucleophilic Displacement
2. Radical-catalyzed Additions to α,β-Unsaturated Boronic Esters1,2
3. .alpha.-Chloro boronic esters from homologation of boronic esters
4. Directed chiral synthesis with pinanediol boronic esters
5. Boronic ester homologation with 99% chiral selectivity and its use in syntheses of the insect pheromones (3S,4S)-4-methyl-3-heptanol and exo-brevicomin
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1. Matteson Homologation-Based Total Synthesis of Meliponamycin A;Organic Letters;2023-12-26
2. Efficient Synthesis of α-Haloboronic Esters via Cu-Catalyzed Atom Transfer Radical Addition;Journal of the American Chemical Society;2023-12-06
3. Stereoselective Synthesis of Secondary and Tertiary Boronic Esters via Matteson Homologation;Organic Letters;2023-09-11
4. Isomerization-Free Matteson Homologations of Substituted Allylboronic Esters;Organic Letters;2023-08-02
5. Enantioselective Construction of Carbocyclic and Heterocyclic Tertiary Boronic Esters by Conjunctive Cross-Coupling Reaction;Journal of the American Chemical Society;2023-07-24
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