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An iodoetherification-dehydroiodination strategy for the synthesis of complex spiroketals from dihydroxyalkene precursors.


ABSTRACT: Dihydroxyalkenes or their monoprotected alcohol derivatives are transformed to 5,5- and 5,6-spiroketals through a sequence involving an initial iodocyclization, followed by a silver triflate mediated spiroketalization step on the derived hydroxy-iodoether.

SUBMITTER: Tony KA 

PROVIDER: S-EPMC3395191 | biostudies-literature | 2008 Apr

REPOSITORIES: biostudies-literature

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An iodoetherification-dehydroiodination strategy for the synthesis of complex spiroketals from dihydroxyalkene precursors.

Tony K A KA   Li Xiaohua X   Dabideen Darrin D   Li Jialiang J   Mootoo David R DR  

Organic & biomolecular chemistry 20080222 7


Dihydroxyalkenes or their monoprotected alcohol derivatives are transformed to 5,5- and 5,6-spiroketals through a sequence involving an initial iodocyclization, followed by a silver triflate mediated spiroketalization step on the derived hydroxy-iodoether. ...[more]

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