Recent Synthetic Advances in C–H/N–H Functionalization of 1H-Pyrazoles: Diverse Strategies Across Variously Substituted Scaffolds

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F25%3A73634926" target="_blank" >RIV/61989592:15310/25:73634926 - isvavai.cz</a>
Result on the web
<a href="https://onlinelibrary.wiley.com/doi/epdf/10.1002/tcr.202500024" target="_blank" >https://onlinelibrary.wiley.com/doi/epdf/10.1002/tcr.202500024</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/tcr.202500024" target="_blank" >10.1002/tcr.202500024</a>

Result language
angličtina
Original language name
Recent Synthetic Advances in C–H/N–H Functionalization of 1H-Pyrazoles: Diverse Strategies Across Variously Substituted Scaffolds
Original language description
This review briefly and systematically overviews C–H and N–H functionalization reactions of pyrazoles, aimed at creating new CC and Cheteroatom bonds on the pyrazole ring. It discusses various strategies, including traditional cross-coupling reactions that necessitate prefunctionalized pyrazoles as well as direct functionalization reactions, which offer a more efficient approach to obtaining a diverse array of functionalized derivatives in only one step.
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
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2025
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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