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Synthesis 2021; 53(23): 4449-4460
DOI: 10.1055/a-1548-8362
DOI: 10.1055/a-1548-8362
paper
Nickel-Catalyzed Hydrodeoxygenation of Aryl Sulfamates with Alcohols as Mild Reducing Agents
This research was supported by JSPS KAKENHI (18K06582, 19K16317, and 19K05459) and Research Grant for Pharmaceutical Sciences from Takeda Science Foundation.

Abstract
The nickel-catalyzed hydrodeoxygenation of aryl sulfamates has been developed with alcohols as mild reductants. A variety of functional groups and heterocycles were tolerated in this reaction system to give the desired products in high yields. In addition, the gram-scale process and stepwise cine-substitution were also achieved with high efficiency.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-1548-8362. Copies of the 1H and 13C NMR spectra are included.
- Supporting Information
Publikationsverlauf
Eingereicht: 14. Juni 2021
Angenommen nach Revision: 13. Juli 2021
Accepted Manuscript online:
13. Juli 2021
Artikel online veröffentlicht:
17. August 2021
© 2021. Thieme. All rights reserved
Georg Thieme Verlag KG
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Reviews:
Reviews:
Triflates and related groups:
Mesylates and tosylates:
Esters:
Carbamates:
Pyridyl ethers and cyanurates:
ortho-Functionalization:
C–C Bond formation:
C-Heteroatom bond formation: