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
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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