Diastereoselective B(C6F5)3-Catalyzed Reductive Carbocyclization of Unsaturated Carbohydrates
Author:
Affiliation:
1. Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States
2. Department of Chemistry, Elon University, Elon, North Carolina 27244, United States
Funder
Basic Energy Sciences
University of North Carolina at Chapel Hill
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b02050
Reference62 articles.
1. Tris(pentafluorophenyl)boron-Catalyzed Hydrosilation of Aromatic Aldehydes, Ketones, and Esters
2. Studies on the Mechanism of B(C6F5)3-Catalyzed Hydrosilation of Carbonyl Functions
3. Conclusive Evidence for an SN2-Si Mechanism in the B(C6F5)3-Catalyzed Hydrosilylation of Carbonyl Compounds: Implications for the Related Hydrogenation
4. Selective Reduction of Carboxylic Acids to Aldehydes Catalyzed by B(C6F5)3
5. Metal-Free Reduction of Secondary and Tertiary N-Phenyl Amides by Tris(pentafluorophenyl)boron-Catalyzed Hydrosilylation
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