An efficient strategy for the modification of α-cyclodextrin: direct conversion of one or two adjacent 6-OHs to phthalimides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Methods for Selective Modifications of Cyclodextrins
2. Phthalimide resin reagent for efficient mitsunobu amino-dehydroxylation
3. PROGRESS IN THE MITSUNOBU REACTION. A REVIEW
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1. Three‐in‐One: Miniature Models of Natural Acyl‐Transfer Systems Enable Vector‐Selective Reaction on the Primary Side of Cyclodextrins;Chemistry – A European Journal;2022-01-10
2. Mono-6-Substituted Cyclodextrins—Synthesis and Applications;Molecules;2021-08-21
3. Enhanced single-isomer separation and pseudoenantiomer resolution of new primary rim heterobifunctionalized α-cyclodextrin derivatives;Beilstein Journal of Organic Chemistry;2018-11-13
4. Functionalised cyclodextrin-based metal–organic frameworks;Chemical Communications;2017
5. Site-Selective Heterofunctionalization of Cyclodextrins: Discovery, Development, and Use in Catalysis;Synlett;2013-10-14
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