One‐Pot Sequential Photoredox Chemistry and Asymmetric Transfer Hydrogenation with a Single Catalyst. Xiao, Z., Jie, Q., Xiaoqiang, H., & Eric, M. European Journal of Organic Chemistry, 2018(4):571–577, January, 2018. Publisher: Wiley-Blackwell
One‐Pot Sequential Photoredox Chemistry and Asymmetric Transfer Hydrogenation with a Single Catalyst [link]Paper  doi  abstract   bibtex   
A sequential process is reported, in which different photoredox reactions are placed in sequence with asymmetric transfer hydrogenations of aryl ketones to provide a diverse set of chiral alcohols with enantioselectivities of up to 99?% ee. The method relies on a single chiral?at?metal catalyst which is added at the beginning of the two step sequence and only a final purification of the reaction product is required.
@article{xiao_onepot_2018,
	title = {One‐{Pot} {Sequential} {Photoredox} {Chemistry} and {Asymmetric} {Transfer} {Hydrogenation} with a {Single} {Catalyst}},
	volume = {2018},
	issn = {1434-193X},
	url = {https://doi.org/10.1002/ejoc.201701652},
	doi = {10.1002/ejoc.201701652},
	abstract = {A sequential process is reported, in which different photoredox reactions are placed in sequence with asymmetric transfer hydrogenations of aryl ketones to provide a diverse set of chiral alcohols with enantioselectivities of up to 99?\% ee. The method relies on a single chiral?at?metal catalyst which is added at the beginning of the two step sequence and only a final purification of the reaction product is required.},
	number = {4},
	journal = {European Journal of Organic Chemistry},
	author = {Xiao, Zhang and Jie, Qin and Xiaoqiang, Huang and Eric, Meggers},
	month = jan,
	year = {2018},
	note = {Publisher: Wiley-Blackwell},
	keywords = {Asymmetric transfer hydrogenation, Chiral‐at‐metal, One‐pot reaction, Photoredox, Sequential catalysis},
	pages = {571--577},
}

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