Palladium/zinc co-catalyzed asymmetric transfer hydrogenation of oxabenzonorbornadienes with alcohols as hydrogen sourcesElectronic supplementary information (ESI) available: Experimental procedures, product characterization, copies of HPLC, 1H and 13C NMR spectra. CCDC 1508992 and 1526719. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ob00175d
Asymmetric transfer hydrogenation of oxabenzonorbornadienes was realized by using alcohols as hydrogen sources under a co-catalytic system of palladium and zinc. Both primary and secondary alcohols could serve as reductants and afforded enantiomerically enriched 1,2-dihydronaphth-1-ol products with...
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creator | Ma, Fujie Chen, Jingchao Yang, Fan Shinde, Madhuri Vikas Zhou, Yongyun Fan, Baomin |
description | Asymmetric transfer hydrogenation of oxabenzonorbornadienes was realized by using alcohols as hydrogen sources under a co-catalytic system of palladium and zinc. Both primary and secondary alcohols could serve as reductants and afforded enantiomerically enriched 1,2-dihydronaphth-1-ol products with high optical purities.
Asymmetric transfer hydrogenation of oxabenzonorbornadienes was realized by using alcohols as hydrogen sources under a co-catalytic system of palladium and zinc. |
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Asymmetric transfer hydrogenation of oxabenzonorbornadienes was realized by using alcohols as hydrogen sources under a co-catalytic system of palladium and zinc.</abstract><doi>10.1039/c7ob00175d</doi><tpages>4</tpages></addata></record> |
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title | Palladium/zinc co-catalyzed asymmetric transfer hydrogenation of oxabenzonorbornadienes with alcohols as hydrogen sourcesElectronic supplementary information (ESI) available: Experimental procedures, product characterization, copies of HPLC, 1H and 13C NMR spectra. CCDC 1508992 and 1526719. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7ob00175d |
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