Highly diastereo- and enantioselective organocatalytic synthesis of trifluoromethylated erythritols based on the in situ generation of unstable trifluoroacetaldehyde
Author:
Affiliation:
1. Department of Chemistry and Biomolecular Science
2. Gifu University
3. Gifu 501-1193
4. Japan
5. Division of Instrumental Analysis
6. Life Science Research Centre
Abstract
A highly diastereo- and enantioselective organocatalytic method to synthesise erythritols bearing a trifluoromethyl group has been investigated.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02067B
Reference48 articles.
1. Erythritol Attenuates Postprandial Blood Glucose by Inhibiting α-Glucosidase
2. Diastereoselective Passerini Reaction of Biobased Chiral Aldehydes: Divergent Synthesis of Various Polyfunctionalized Heterocycles
3. A General Strategy for the Discovery of Metabolic Pathways: d-Threitol, l-Threitol, and Erythritol Utilization in Mycobacterium smegmatis
4. Synthesis of Methylerythritol Phosphate Analogues and Their Evaluation as Alternate Substrates for IspDF and IspE from Agrobacterium tumefaciens
5. Efficient asymmetric organocatalytic formation of erythrose and threose under aqueous conditions
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