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In subsequent studies it was found that alkylation of C24-OTBS ascomycin (9) with methylstyrenyl-2,2,2- trichloroacetimidate (10) followed by Johnson-Lemieux oxidation could provide 6 in good yield and without the requirement of carbon-carbon bond formation. (Formula Presented)
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0009571241
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1H NMR (400 MHz) and mass spectral data were obtained on all reaction products.
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0009571036
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50's generated within a single experiment set (n = 3).
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Preparation: 1. acylation of C24-OTBS ascomycin with phenylacetyl chloride; 2. desilylation (HF•pyr).
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19
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0009571656
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Parsons, W.H.13
Wyvratt, M.J.14
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