Stereoselective synthesis of (−)-3-PPP through palladium-catalysed unactivated C(sp3)-H arylation at the C-3 position of l-pipecolinic acid
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文摘
An efficient route for the preparation of (−)-3-PPP is described. The chiral center formed in the key reaction was completely induced by the adjacent stereocenter of the substrate. Substitution effect of nitrogen on the efficiency of the key reaction was explored with substantial experiments.

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