Diastereoselective Synthesis Of A Spironoraristeromycin Using An Acylnitroso Diels-Alder Reaction

JOURNAL OF ORGANIC CHEMISTRY(2009)

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摘要
The tert-butyl N-hydroxycarbamate-derived nitroso reagent I reacted with N-Cbz-protected spirocyclic diene 2 to provide spirocycloadduct 3. Here we describe the efficient conversion of 3 into the novel carbocyclic nucleoside spironoraristeromycin 4.
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organic chemistry
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