Total Stereoselective Michael Addition of N- and S- Nucleophiles to a d-Erythrosyl 1,5-Lactone Derivative. Experimental and Theoretical Studies Devoted to the Synthesis of 2,6-Dideoxy-4-functionalized-d-ribono-hexono-1,4-lactone
Author:
Affiliation:
1. REQUIMTE/UCIBIO, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre s/n, 4169-007 Porto, Portugal
2. Departamento de Química, Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal
Funder
European Regional Development Fund
Funda??o para a Ci?ncia e a Tecnologia
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b00769
Reference31 articles.
1. Synthesis of Iminosugars from Tetroses
2. Some Oxidation and Reduction Products of 2,4-O-Ethylidene-D-erythrose1
3. (1'R)-(−)-2,4-O-ETHYLIDENE-D-ERYTHROSE AND ETHYL (E)-(−)-4,6-O-ETHYLIDENE-(4S,5R,1'R)-4,5,6-TRIHYDROXY-2-HEXENOATE
4. Synthesis of intermediates in the formation of hydroxy piperidines and 2-azido lactones from d-erythrose
5. Stereocontrolled synthesis of fully functionalized d-glucosamine monosaccharides via a domino nitro-Michael/Henry reaction
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2. A Short Synthesis of (2S,3S,4R)-Dihydroxyhomoprolines from d-Erythrose-Derived 5,6-Dihydro-2H-pyran-2-one;Synthesis;2019-04-15
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