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Axially chiral N-alkyl-N-cinnamoyl amide type P,olefin ligands for Pd-catalyzed reactions†
Kaho Takaya,Kaito Koki,Natsume Akimoto,Yoshio Kasashima
Organic & Biomolecular Chemistry Pub Date : 03/11/2023 00:00:00 , DOI:10.1039/D3OB00224A
Abstract

We synthesized N-alkyl-N-cinnamoyl amide type phosphine–olefin compounds 1 and found axial chirality in a C(aryl)–N(amide) bond in compounds 1 by HPLC analysis using a chiral stationary phase column. We successfully obtained enantiomeric isomers of 1 and demonstrated the use of (–)-1 for chiral ligands in Pd-catalyzed asymmetric allylic substitution reactions of allylic esters with indoles (up to 97% ee).

Graphical abstract: Axially chiral N-alkyl-N-cinnamoyl amide type P,olefin ligands for Pd-catalyzed reactions
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