Journal
SYNTHESIS-STUTTGART
Volume 54, Issue 21, Pages 4753-4763Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/a-1672-6284
Keywords
enantioselectivity; iridium; benzamides; catalysis; C-H activation
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Funding
- Japan Society for the Promotion of Science (JSPS) KAKENHI [JP19H02721, JP20J23499]
- JSPS
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Chiral phosphoramidite-olefin hybrid ligands were effective in the iridium-catalyzed asymmetric alkylation of N-arylbenzamides with vinyl ethers. The reaction yield was high, with high branch selectivity and enantioselectivity.
Chiral phosphoramidite-olefin hybrid ligands were found to be effective in the iridium-catalyzed asymmetric alkylation of N-arylbenzamides with vinyl ethers. The reaction is catalyzed by a hydroxo-iridium catalyst coordinated with the hybrid ligand to give the corresponding products in high yields with high branch selectivity and enantioselectivity.
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