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Ligand-Controlled Copper(I)-Catalyzed Cross-Coupling of Secondary and Primary Alcohols to α-Alkylated Ketones, Pyridines, and Quinolines
Journal article   Peer reviewed

Ligand-Controlled Copper(I)-Catalyzed Cross-Coupling of Secondary and Primary Alcohols to α-Alkylated Ketones, Pyridines, and Quinolines

Da-Wei Tan, Hong-Xi Li, Da-Liang Zhu, Hai-Yan Li, David James Young, Jian-Lin Yao and Jian-Ping Lang
Organic Letters, Vol.20(3), pp.608-611
2018
PMID: 29336159
url
https://doi.org/10.1021/acs.orglett.7b03726View
Published Version

Abstract

One hexanuclear Cu(I) cluster of 4,6-dimethylpyrimidine-2-thiolate efficiently catalyzes the dehydrogenative cross-coupling of secondary and primary alcohols to α-alkylated ketones with high selectivity. This transformation proceeds through a one-pot sequence of dehydrogenation of alcohols, condensation of aldehydes and ketones, hydrogenation of the resulting α,β-unsaturated ketones, and dehydrogenation of the α-alkylated alcohols to generate α-alkylated ketones. This catalytic system also displays high activity for the annulation reaction of secondary alcohols with γ-amino- and 2-aminobenzyl alcohols to yield pyridines and quinolines, respectively.

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Domestic collaboration
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Web Of Science research areas
Chemistry, Organic
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