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Blue-Light-Driven Iron-Catalyzed Desulfurization of Thioamides under Hydrosilylation Conditions
被引:0
|作者:
Zhang, Qingxin
[1
]
Darcel, Christophe
[1
]
机构:
[1] Univ Rennes, CNRS, ISCR, UMR 6226, F-35000 Rennes, France
关键词:
Iron;
Thioamide;
Desulfurization;
Hydrosilylation;
Blue light activation;
SELECTIVE REDUCTION;
ETHANETHIOL ESTERS;
ACID-DERIVATIVES;
TERTIARY AMIDES;
ALDEHYDES;
COMPLEXES;
AMINATION;
FACILE;
AMINES;
TRANSFORMATION;
D O I:
10.1002/ejoc.202500048
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Up to now, there were only few reports on Earth-abundant transition metal catalyzed reductions of thioamides, one of the explanation of this scarcity being the possible metallic catalyst poisoning due to the adsorption of species containing sulfur. In this contribution, we report the first general iron-catalyzed hydrogenative desulfurization of tertiary thioamides under hydrosilylation conditions at ambient temperature, the reaction being driven by blue light irradiation. To perform selectively the reduction of thioamides leading to amines (30 examples, 29-97 % yields), highlighting the sole cleavage of the C=S bond, Fe(IMes)(CO)4 catalyst was used in the presence of phenylsilane under ambient conditions.
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