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Fluorinated terpenoids and their fluorine-containing derivatives
Muhammad Badrul Huda1,2, Nurlelasari1, Unang Supratman1,3
1Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Padjadjaran Jl. Raya Bandung-Sumedang Km 21 Sumedang 45363 West Java Indonesia y.p.budiman@unpad.ac.id.
Fluorinated terpenoids are synthesized using various strategies to enhance drug properties. This review covers methods for creating these unique molecules across different terpene subclasses.
Area of Science:
- Organic Chemistry
- Medicinal Chemistry
- Natural Products Chemistry
Background:
- Fluorine incorporation modifies molecular properties, enhancing pharmaceutical applications.
- Terpenoids are a diverse class of natural products with significant bioactivity.
- Naturally occurring fluorinated organic molecules are rare, driving synthetic interest.
Purpose of the Study:
- To review synthetic strategies for fluorinated terpenoids.
- To cover fluorination across various terpene subclasses (mono-, sesqui-, di-, tri-, tetranor-terpenes).
- To highlight the potential of fluorinated terpenoids in drug discovery.
Main Methods:
- Summarization of existing synthetic methodologies.
- Categorization of strategies based on terpene subclass.
- Analysis of approaches for introducing fluorine into terpenoid structures.
Main Results:
- Diverse synthetic routes exist for preparing fluorinated terpenoids.
- Fluorination can modulate the bioactivity of terpenoid scaffolds.
- The review encompasses a wide range of terpene structures.
Conclusions:
- Synthetic fluorination is key to expanding the utility of terpenoids in medicine.
- Developing efficient fluorination methods is crucial for accessing novel drug candidates.
- Fluorinated terpenoids offer promising avenues for pharmaceutical research.
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