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Organocatalytic Enantio- and Diastereoselective Acetalization of δ-Oxoenones via Cyanohydrin Formation

机译:通过氰醇形成的δ-氧代酮的有机催化和非对映选择性缩醛化

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摘要

Due to the ubiquity in biologically active natural products and pharmaceuticals, chiral 1,3-diols have been gathered much attention as attractive synthetic targets. Although a number of stereoselective multistep syntheses of these structures have been reported to date, simultaneous catalytic construction of two stereogenic centers of chiral 1,3-diol structures is still challenging;; especially an approach to syn-1,3-diol motifs from achiral substrates with high level of stereocontrol remains unexploited.
机译:由于生物活性天然产物和药物中的难以致力于,手性1,3-二醇已被充分地关注有吸引力的合成靶标。虽然已经报道了这些结构的许多立体选择性多体合成,但同时催化构建手性1,3-二醇结构的两个立体型中心仍然具有挑战性;特别是具有高水平立体控制的成立基材的同步1,3-二醇图案的方法仍未爆发。

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