Novel rearrangement reactions in the fluorination of methyl 3-C-methyl-3-nitro-α-l-hexopyranosides by the DAST reagent
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Chemistry and Developments of Fluorinated Carbohydrates
2. Assignment of the 1H, 19F, and 13C NMR spectra of 2-deoxy-2-fluoro-d-ribose and characterisation of the isomeric equilibrium
3. Synthesis of 2'-C-.beta.-fluorodaunomycin. An example of configurational retention in fluorodehydroxylation with diethylaminosulfur trifluoride
4. Stereospecific 1,2-migrations in carbohydrates. Stereocontrolled synthesis of .alpha.- and .beta.-2-deoxyglycosides
5. The Reaction of Methyl 3-O-Benzyl-4, 6-O-benzylidene-α-D-mannopyranqside with Diethylaminosulfur Trifluoride (DAST)
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1. Structural modification of oridonin via DAST induced rearrangement;RSC Advances;2018
2. Synthesis and Glycosidase Inhibition of Australine and Its Fluorinated Derivatives;Organic Letters;2015-01-26
3. DAST-promoted Beckmann rearrangement/intramolecular cyclization of acyclic ketoximes: access to 2-oxazolines, benzimidazoles and benzoxazoles;Chemical Communications;2015
4. Synthesis of cyclically constrained sugar derived α/β- and α/γ-peptides;Org. Biomol. Chem.;2013
5. A versatile and convenient route to ketone C-pyranosides and ketone C-furanosides from unprotected sugars;Tetrahedron;2012-01
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