Diisobutylaluminum Hydride Mediated Regioselective O Desilylations: Access to Multisubstituted Cyclodextrins
Cyclodextrins
Molecular Conformation
Organometallic Compounds
Stereoisomerism
Silanes
01 natural sciences
0104 chemical sciences
DOI:
10.1002/anie.201105737
Publication Date:
2011-10-18T07:31:43Z
AUTHORS (4)
ABSTRACT
A face off: Diisobutylaluminum hydride (DIBAL-H) has been found to be an effective O-desilylating reagent at the primary of cyclodextrins. This methodology shows high chemo- and regioselectivity provides route orthogonally protected, multisubstituted cyclodextrin derivatives.
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