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- W2171410720 abstract "P,N-ligands trans-4 and cis-5 with a cyclohexane backbone were easily synthesized. The key step was chiral resolution of (±)-trans-2-pyridylcyclohexanols with DBTA. Enantiopure trans isomer was subjected to Mitsunobu reaction and deprotection to give the corresponding cis isomer. These ligands have been successfully used in asymmetric hydrogenation of arylalkenes with up to 93% ee using 5 and 90% ee using 4 and asymmetric allylic alkylations with up to 95% ee using 5 and 93% ee using 4. Trans and cis P,N-ligands 4 and 5 all gave the product with the same configuration. It was suggested that the absolute configuration of the product was controlled by the configuration of the stereogenic pyridyl-bearing carbon of the ligands." @default.
- W2171410720 created "2016-06-24" @default.
- W2171410720 creator A5015288133 @default.
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- W2171410720 date "2007-03-01" @default.
- W2171410720 modified "2023-10-17" @default.
- W2171410720 title "Synthesis of chiral cyclohexane-backbone P,N-ligands derived from pyridine and their applications in asymmetric catalysis" @default.
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- W2171410720 doi "https://doi.org/10.1016/j.tetlet.2007.01.123" @default.
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