The intramolecular stabilizing effects of O-benzoyl substituents as a driving force of the acid-promoted pyranoside-into-furanoside rearrangement

Alexey G. Gerbst, Sofya P. Nikogosova, Darya A. Rastrepaeva, Dmitry A. Argunov, Vadim B. Krylov and Nikolay E. Nifantiev
Beilstein J. Org. Chem. 2025, 21, 2456–2464. https://doi.org/10.3762/bjoc.21.187

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The intramolecular stabilizing effects of O-benzoyl substituents as a driving force of the acid-promoted pyranoside-into-furanoside rearrangement
Alexey G. Gerbst, Sofya P. Nikogosova, Darya A. Rastrepaeva, Dmitry A. Argunov, Vadim B. Krylov and Nikolay E. Nifantiev
Beilstein J. Org. Chem. 2025, 21, 2456–2464. https://doi.org/10.3762/bjoc.21.187

How to Cite

Gerbst, A. G.; Nikogosova, S. P.; Rastrepaeva, D. A.; Argunov, D. A.; Krylov, V. B.; Nifantiev, N. E. Beilstein J. Org. Chem. 2025, 21, 2456–2464. doi:10.3762/bjoc.21.187

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Scholarly Works

  • Gerbst, A. G.; Argunov, D. A.; Krylov, V. B.; Nifantiev, N. E. The Computational Study of the Mechanism of the Acid-Promoted Pyranoside-into-Furanoside Rearrangement. Molecules (Basel, Switzerland) 2026, 31, 3145. doi:10.3390/molecules31183145
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