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Short Note

Allobetulin

by 1,2,3,* and 1,2,*
1
Department of Organic Chemistry, Bioorganic Chemistry and Biotechnology, Silesian University of Technology, B. Krzywoustego 4, 44-100 Gliwice, Poland
2
Biotechnology Center, Silesian University of Technology, B. Krzywoustego 8, 44-100 Gliwice, Poland
3
Department of Chemical Organic Technology and Petrochemistry, Silesian University of Technology, B. Krzywoustego 4, 44-100 Gliwice, Poland
*
Authors to whom correspondence should be addressed.
Academic Editor: Luke R. Odell
Molbank 2022, 2022(3), M1446; https://doi.org/10.3390/M1446
Received: 2 September 2022 / Revised: 9 September 2022 / Accepted: 13 September 2022 / Published: 15 September 2022
(This article belongs to the Section Organic Synthesis)
Allobetulin was synthesized at room temperature, starting from betulin by Wagner–Meerwein rearrangement in the presence of tetrafluoroboric acid diethyl ether complex. The structure of the compound obtained was confirmed by spectroscopic methods (1H, 13C NMR and IR). View Full-Text
Keywords: triterpenoids; betulin; allobetulin; Wagner–Meerwein rearrangement triterpenoids; betulin; allobetulin; Wagner–Meerwein rearrangement
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MDPI and ACS Style

Grymel, M.; Adamek, J. Allobetulin. Molbank 2022, 2022, M1446. https://doi.org/10.3390/M1446

AMA Style

Grymel M, Adamek J. Allobetulin. Molbank. 2022; 2022(3):M1446. https://doi.org/10.3390/M1446

Chicago/Turabian Style

Grymel, Mirosława, and Jakub Adamek. 2022. "Allobetulin" Molbank 2022, no. 3: M1446. https://doi.org/10.3390/M1446

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