((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-Acetoxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-3aH-cyclopenta[a]chrysen-3a-yl)methyl 2-Bromo-3-methylbenzoate

In this report, we discuss the synthesis of modified betulin through the chemical derivatization of a natural compound. The compound was fully characterized by proton (1H), carbon-13 (13C), heteronuclear single quantum coherence (HSQC) and distortionless enhancement through polarization transfer (DEPT) NMR and elemental analysis. We investigated the optical properties through ultraviolet (UV) and Fourier-transform infrared (FTIR) spectroscopy.

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Publication Details

Journal
Molbank
Published
2025-02-20
DOI
https://doi.org/10.3390/m1971
Citations
1
Primary Topic
Natural product bioactivities and synthesis
Type
article
Field-Weighted Citation Impact
0.81

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article

((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-Acetoxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-3aH-cyclopenta[a]chrysen-3a-yl)methyl 2-Bromo-3-methylbenzoate

Paolo Coghi, Carmine Coluccini, Yuzhu Guo, Yang Xiao
1 citations
Molbank
Natural product bioactivities and synthesis
0.81
article

((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-Acetoxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-3aH-cyclopenta[a]chrysen-3a-yl)methyl 2-Bromo-3-methylbenzoate

Paolo Coghi, Carmine Coluccini, Yuzhu Guo, Yang Xiao
article en
1 citations

Abstract

In this report, we discuss the synthesis of modified betulin through the chemical derivatization of a natural compound. The compound was fully characterized by proton (1H), carbon-13 (13C), heteronuclear single quantum coherence (HSQC) and distortionless enhancement through polarization transfer (DEPT) NMR and elemental analysis. We investigated the optical properties through ultraviolet (UV) and Fourier-transform infrared (FTIR) spectroscopy.

MolbankVol. 2025(1)
Macau University of Science and Technology (MO), China Medical University (TW)
Ministry of Science and Technology, Taiwan, Fundo para o Desenvolvimento das Ciências e da Tecnologia
Openalex Percentile: Top 31%
Natural product bioactivities and synthesis
0.81
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