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. Stereoselective Synthesis of α‐Azido Esters and α‐Amino Acid Derivatives via Matteson Homologation of Boronic Esters;Zeitschrift für anorganische und allgemeine Chemie;2024-09-03
2. Synthesis and Suzuki–Miyaura Cross-Coupling of Alkyl Amine-Boranes. A Boryl Radical-Enabled Strategy;Journal of the American Chemical Society;2024-08-13
3. Stereospecific alkenylidene homologation of organoboronates by SNV reaction;Nature;2024-05-23
4. Flow Chemistry of Metal Carbenoid Species towards Selective Organic Synthesis;Synthesis;2024-04-09
5. Synthesis and Late-Stage Modification of (−)-Doliculide Derivatives Using Matteson’s Homologation Approach;Marine Drugs;2024-04-08
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