Synthesis and Structure Confirmation of Selagibenzophenone C

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F22%3A10444107" target="_blank" >RIV/00216208:11310/22:10444107 - isvavai.cz</a>
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=P.0x8Kcjxk" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=P.0x8Kcjxk</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ejoc.202200014" target="_blank" >10.1002/ejoc.202200014</a>

Result language
angličtina
Original language name
Synthesis and Structure Confirmation of Selagibenzophenone C
Original language description
We report the first total synthesis of natural diarylbenzophenone selagibenzophenone C recently isolated from a plant species Selaginella tornanscina, traditionally used in folklore medicines. The framework of the natural compound is assembled via Suzuki-Miyaura cross-coupling and the addition of organometallic species. Following some ambiguities in the assignment of the structures for some of the natural products belonging to this compound class, the spectral data reported for the isolated selagibenzophenone C are carefully compared to the data of the synthetic product, and the structure of the natural product is confirmed.
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
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OECD FORD branch
10401 - Organic chemistry

Project
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Continuities
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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