Olean-18α-19β,28-epoxy-3β-benzoate

Allobetulin 3-benzoate was obtained as an unexpected byproduct during the acid-mediated protection–deprotection of betulin. Single-crystal X-ray diffraction analysis shows that it crystallizes in the triclinic space group P1 with Z = 2 and contains two crystallographically independent molecules in the asymmetric unit. Compared with allobetulin (P21, Z = 4) and allobetulin 3-acetate (C2, Z = 4), the benzoyl substitution at C-3 induces distinct molecular packing and intermolecular interaction patterns, highlighting the influence of steric and electronic effects on crystal architecture.

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Publication Details

Journal
Molbank
Published
2026-07-01
DOI
https://doi.org/10.3390/m2197
Primary Topic
Natural product bioactivities and synthesis
Type
article
Field-Weighted Citation Impact
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article

Olean-18α-19β,28-epoxy-3β-benzoate

Y N Wang, Lak Shin Jeong, Qiang Wang, Bohua Lu et al.
Molbank
Natural product bioactivities and synthesis
article

Olean-18α-19β,28-epoxy-3β-benzoate

Y N Wang, Lak Shin Jeong, Qiang Wang, Bohua Lu, Xiaoyi Sun, Jinxing Zhai, Jung Hoon Park, Xiqiang Gao
article en

Abstract

Allobetulin 3-benzoate was obtained as an unexpected byproduct during the acid-mediated protection–deprotection of betulin. Single-crystal X-ray diffraction analysis shows that it crystallizes in the triclinic space group P1 with Z = 2 and contains two crystallographically independent molecules in the asymmetric unit. Compared with allobetulin (P21, Z = 4) and allobetulin 3-acetate (C2, Z = 4), the benzoyl substitution at C-3 induces distinct molecular packing and intermolecular interaction patterns, highlighting the influence of steric and electronic effects on crystal architecture.

MolbankVol. 2026(4)
Seoul National University (KR), Henan University of Technology (CN), Henan Academy of Sciences (CN)
Openalex Percentile: Top 11%
Natural product bioactivities and synthesis
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