Title of article
Using click chemistry to access mono- and ditopic β-cyclodextrin hosts substituted by chiral amino acids Original Research Article
Author/Authors
Diem Ngan Tran، نويسنده , , Claire Blaszkiewicz، نويسنده , , Stéphane Menuel، نويسنده , , Alain Roucoux، نويسنده , , Karine Philippot، نويسنده , , Frédéric Hapiot، نويسنده , , Eric Monflier، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2011
Pages
9
From page
210
To page
218
Abstract
A wide range of chiral mono- and ditopic cyclodextrin-based receptors have been synthesized by CuI-catalyzed azide–alkyne cycloaddition starting from mono-6-azido-β-cyclodextrin and chiral amino acids. Of interest, microwaves proved very efficient to access a wide range of ditopic β-cyclodextrin receptors with quantitative yields.
Keywords
Cyclodextrins , Azides , Amino acids , Cycloaddition , Chirality
Journal title
Carbohydrate Research
Serial Year
2011
Journal title
Carbohydrate Research
Record number
966835
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