Ring-Expansion Induced 1,2-Metalate Rearrangements: Highly Diastereoselective Synthesis of Cyclobutyl Boronic Esters
Author:
Affiliation:
1. School of Chemistry, University of Bristol, Cantock’s Close, Bristol BS8 1TS, U.K.
Funder
Engineering and Physical Sciences Research Council
H2020 Marie Sklodowska-Curie Actions
UCB UK
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.0c00813
Reference40 articles.
1. The development of a simple general procedure for synthesis of pure enantiomers via chiral organoboranes
2. Boronic Esters in Asymmetric Synthesis
3. Homologation and alkylation of boronic esters and boranes by 1,2-metallate rearrangement of boron ate complexes
4. Stereospecific functionalizations and transformations of secondary and tertiary boronic esters
5. Lithiation–Borylation Methodology and Its Application in Synthesis
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