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Stereochemical Diversity through Cyclodimerization: Synthesis of Polyketide-like Macrodiolides

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NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Stereochemical_Diversity_through_Cyclodimerization_Synthesis_of_Polyketide-like_Macrodiolides/3746973
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An expeditious procedure for the direct formation of stereochemically well-defined macrodiolides is described. Cyclodimerizations of enantioenriched C7 and C8 hydroxy esters 6 in the presence of catalytic amounts of distannoxane transesterification catalysts afford 14- to 22-membered macrodiolides 7−9 bearing up to six stereocenters. Additional structural diversity is introduced by further stereoselective reactions on selected macrodiolides 7a, 7g, 10a, and 11.
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2016-08-20
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