A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups
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An alpha-cyclodextrin protected with 2,4-dichlorobenzyl groups on the primary alcohols and ordinary benzyl groups on the secondary alcohols was prepared and subjected to DIBAL (diisobutylaluminum hydride)-promoted selective debenzylation. Debenzylation proceeded by first removing two dichlorobenzyl groups from the 6A,D positions and then removing one or two benzyl groups from the 3A,D positions.
Originalsprog | Engelsk |
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Tidsskrift | Beilstein Journal of Organic Chemistry |
Vol/bind | 18 |
Sider (fra-til) | 1553-1559 |
Antal sider | 7 |
ISSN | 1860-5397 |
DOI | |
Status | Udgivet - 17 nov. 2022 |
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