First selective synthesis of thio-β-cyclodextrin derivatives by a direct mitsunobu reaction on free β-cyclodextrin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Mitsunobu Thiofunctionalization-Part 2.1an Expedient Synthesis of Aza-Heterocycle/Thiosugar Hybrids
2. Efficient Synthesis of Deoxy and Dideoxy Sugars by a Thio-Mitsunobu Reaction on Unprotected Glycosides
3. Synthesis of 6-Deoxy and 3,6-Dideoxy Derivatives from Unprotected Glycosides Employing the Mitsunobu Reaction
4. α-d-mannosyl- and β-d-galactosyl derivatives of cyclodextrins.
5. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
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3. Selective modifications at the different positions of cyclodextrins: a review ofstrategies;TURKISH JOURNAL OF CHEMISTRY;2020-04-01
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