Photochemical C-H Amination of Ethers and Geminal Difunctionalization Reactions in One Pot

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F19%3A00508815" target="_blank" >RIV/61388963:_____/19:00508815 - isvavai.cz</a>
Result on the web
<a href="https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201905209" target="_blank" >https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201905209</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/anie.201905209" target="_blank" >10.1002/anie.201905209</a>

Result language
angličtina
Original language name
Photochemical C-H Amination of Ethers and Geminal Difunctionalization Reactions in One Pot
Original language description
A mild, atom-economic, and metal-free alpha-C-H amination of ethers using relatively stable nonafluorobutanesulfonyl (nonaflyl, Nf) azide as the aminating reagent to give N-sulfonyl hemiaminals is reported. This enables unprecedented C(sp(3)) difunctionalization reactions, leading to diverse functionalized amino group containing compounds starting from simple ethers in one pot.
Czech name
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Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10401 - Organic chemistry

Project
<a href="/en/project/GA17-14510S" target="_blank" >GA17-14510S: Photochemical C-H amination reactions of hydrocarbons, ethers, sulfides or tertiary amines and their applications in organic chemistry</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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