Synthesis of tetrahydropyrans from sugar lactones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Ring contraction of 3-deoxy-2-O-trifluoromethanesulphonates of α-hydroxy-γ-lactones to oxetanes
2. The ring contraction of δ-lactones with leaving group α-substituents: a strategy for the synthesis of 2,5-disubstituted highly functionalised homochiral tetrahydrofurans
3. Acid-catalysed transformation of α-trifluoromethanesulfonates of γ- and δ-lactones into 2,5-disubstituted homochiral tetrahydrofurans
4. Tetrahydropyran derivatives from γ- and δ-hexonolactones
5. Useful Designs in the Synthesis of Trans-Fused Polyether Toxins
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3. d - and l - altro - C -furanosides (II/ ent -II, α- C -Lyxose, α- C -Ribose);C-Furanosides;2018
4. Stereodirected reactions of salicilaldehyde derivatives with tert-butyl 3(4)-hydroxy-2(3)-(3-methylbut-2-enyl)- piperidine-1-carboxylates as an efficient preparation procedure of tetrahydropyran derivatives fused with a piperidine ring;Russian Journal of Organic Chemistry;2016-08
5. Unprecedented 3- O -methyl-3- C -trifluoromethyl- d -ribono- (and l -lyxono)-γ-lactones synthesized by nucleophilic trifluoromethylation of d -hexose-derived cyclic ketones;Journal of Fluorine Chemistry;2016-06
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