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Conformational preferences of zampanolide and dactylolide.

ORGANIC LETTERS(2013)

Cited 15|Views2
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Abstract
The solution conformation behavior of the macrolide core of microtubule-stabilizing agents (-)-zampanolide and (-)-dactylolide has been determined through a combination of high-field NMR experiments and computational modeling. Taken together, the results demonstrate that in solution both molecules exist as a mixture of three interconverting conformational families, one of which bears strong resemblance to zampanolide's tubulin-bound conformation.
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Key words
stereoisomerism,magnetic resonance spectroscopy,monte carlo method
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