| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5228159 | Tetrahedron | 2008 | 5 Pages |
Abstract
The Cu(I)-catalyzed azide-alkyne cycloaddition has enabled practical and efficient preparation of hydroxylated, permethylated and peracylated β-cyclodextrin dimers in good yields starting from mono-6-azido-β-cyclodextrin and ortho-, meta- or para-bis-(prop-2-ynyloxy)benzenes as spacers.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Maxime Mourer, Frédéric Hapiot, Eric Monflier, Stéphane Menuel,