Peptide-Catalyzed Diastereo- and Enantioselective Cyclopropanation of Aromatic 伪,尾-Unsaturated Aldehydes
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文摘
Highly diastereo- and enantioselective cyclopropanation of aromatic 伪,尾-unsaturated aldehydes was achieved using a resin-supported peptide catalyst under aqueous conditions. In the peptide sequence, the residue possessing an oxygen atom with the appropriate length of the side chain was essential for attaining good diastereoselectivity.

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