Catalytic Asymmetric Vinylogous Mannich-type (AVM) Reaction of Nonactivated 伪-Angelica Lactone
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文摘
A direct highly diastereo- and enantioselective asymmetric vinylogous Mannich-type (AVM) reaction of aldimines with nonactivated natural 伪-angelica lactone has been successfully developed. It was demonstrated that the nonactivated natural 伪-angelica lactone is a useful vinylogous nucleophile to give the chiral 未-amino 纬,纬-disubstituted butenolide carbonyl derivatives. The N,N鈥?/i>-dioxide L2鈥揝cIII complex is efficient toward the obtention of a range of corresponding products with adjacent quaternary and tertiary stereocenters in excellent dr and ee values.

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