Ferrier Reaction: The first synthesis of 2,3-unsaturated seleno-glycosides by using alkyl(aryl) hydroselenides as the nucleophile and Hf(OTf)4 as the catalyst
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference32 articles.
1. Use of a phenyl 1-selenogalactofuranoside as a glycosyl donor for the synthesis of galactofuranosyl-containing disaccharides
2. Synthesis of galactofuranosyl-containing oligosaccharides corresponding to the glycosylinositolphospholipid of Trypanosomacruzi
3. A concise synthesis of the O-glycosylated amino acid building block; using phenyl selenoglycoside as a glycosyl donor
4. Synthesis of erythro and threo furanoid glycals from 1- and 2-phenylselenenyl–carbohydrate derivatives
5. Elimination reactions of glycosyl selenoxides
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1. Recent Progress in Synthetic and Biological Application of Diorganyl Diselenides;The Chemical Record;2024-07
2. Site-specific synthesis of 3-Se-1,2-unsaturated glycosides with R-Se-Se-R as the nucleophile precursors promoted by InCl3/Hf(OTf)4;Tetrahedron Letters;2021-12
3. Synthesis of Diverse Seleno‐Glycolipids via the Transacetalization of Selenoacetals;European Journal of Organic Chemistry;2021-08-31
4. On-water synthesis of glycosyl selenocyanate derivatives and their application in the metal free organocatalytic preparation of nonglycosidic selenium linked pseudodisaccharide derivatives;RSC Advances;2021
5. Progress in the Synthesis of 2,3-unsaturated Glycosides;Current Organic Chemistry;2020-04-15
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