Asymmetric Access to Boryl-Substituted Vicinal Aminoalcohols through Cu-Catalyzed Reductive Coupling
Author:
Affiliation:
1. Department of Chemistry, Virginia Commonwealth University, 1001 West Main Street, Richmond, Virginia 23284, United States
Funder
Division of Chemistry
Altria Group
Virginia Commonwealth University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c01459
Reference55 articles.
1. Natural Products with Heteroatom-Rich Ring Systems
2. Biocatalytic approaches towards the stereoselective synthesis of vicinal amino alcohols
3. Cheminformatic Analysis of Natural Products and their Chemical Space
4. Multi-step synthesis strategies towards 1,2-amino alcohols with special emphasis on phenylpropanolamines
5. The Synthesis of Vicinal Amino Alcohols
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2. Chiral bisphosphine Ph-BPE ligand: a rising star in asymmetric synthesis;Chemical Society Reviews;2024
3. Development of regiodivergent asymmetric reductive coupling reactions of allenamides to access heteroatom-rich organic compounds;Chemical Communications;2023
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