Selective mono-O-sulfonylation of A,B-di-altro- β-cyclodextrin by utilizing restricted orientation of a guest-type sulfonylating reactant in the elliptically distorted cavity: the 2A-O- and 3G-O-2-naphthalenesulfonates as a versatile scaffold to prepare artificial enzymes with controlling substrate orientation-Reference-Cited by-同舟云学术

Selective mono-O-sulfonylation of A,B-di-altro- β-cyclodextrin by utilizing restricted orientation of a guest-type sulfonylating reactant in the elliptically distorted cavity: the 2A-O- and 3G-O-2-naphthalenesulfonates as a versatile scaffold to prepare artificial enzymes with controlling substrate orientation

Published:2004-09 Issue:37 Volume:45 Page:6899-6902
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fujita Kahee,Chen Wen-Hua,Oiwane Kaori,Fujioka Toshihiro,Fukudome Makoto,Yuan De-Qi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

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2. Biomimetic Reactions Catalyzed by Cyclodextrins and Their Derivatives

3. General method for preparing altrosides from 2,3-manno-epoxides and its application to synthesis of alternative β-cyclodextrin with an altroside as the constituent of macrocyclic structure

4. Guest-induced conformational change in a flexible host: mono-altro-β-cyclodextrin

5. Restriction of guest rotation based on the distortion of a cyclodextrin cavity

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