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Visible-light-promoted aerobic metal-free aminothiocyanation of activated ketones

A direct, redox-neutral, highly atom-economical and metal-free aerobic method for the synthesis of multi-substituted olefins via simply coupling ammonium thiocyanate with activated ketones is described. A series of multi-substituted olefins could be easily and efficiently obtained in excellent yield...

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Bibliographic Details
Published in:Green chemistry : an international journal and green chemistry resource : GC 2018, Vol.20 (24), p.5464-5468
Main Authors: Yuan, Pan-Feng, Zhang, Qing-Bao, Jin, Xiao-Ling, Lei, Wen-Long, Wu, Li-Zhu, Liu, Qiang
Format: Article
Language:English
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Summary:A direct, redox-neutral, highly atom-economical and metal-free aerobic method for the synthesis of multi-substituted olefins via simply coupling ammonium thiocyanate with activated ketones is described. A series of multi-substituted olefins could be easily and efficiently obtained in excellent yields by using low-toxicity and inexpensive ammonium thiocyanate as an amine and thiocyanate source, and water is the only by-product.
ISSN:1463-9262
1463-9270
DOI:10.1039/C8GC02720J