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- W2149805101 abstract "Putting the pieces together: The total synthesis of the natural macrolide oasomycin A has been realized. Key fragment couplings include an anti-Felkin selective aldol addition (green), Kociensky–Julia olefinations (red), and competitive Weinreb amide acylation reaction (blue). The utility of the 4,5-diphenyloxazole as a carboxy surrogate and the late-stage macrolactonization affording the 42-membered macrocycle of oasomycin A are also described. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2007/z603652_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2149805101 date "2007-01-10" @default.
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- W2149805101 title "Enantioselective Synthesis of Oasomycin A, Part III: Fragment Assembly and Confirmation of Structure" @default.
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- W2149805101 doi "https://doi.org/10.1002/anie.200603652" @default.
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