# Structural Modifications at the C3 and C30 Positions of the Lupane Skeleton with Carbon-Centered Nucleophiles

## TL;DR

This paper describes the chemical modification of lupeol, a plant compound, by altering specific positions in its structure to create new derivatives.

## Contribution

The study introduces new methods for stereoselective alkylation at C3 and oxidative modification at C30 of the lupane skeleton.

## Key findings

- Fourteen lupeol derivatives were synthesized through selective functionalization at C3 and C30 positions.
- Stereoselective alkylation at C3 was achieved using various carbanions.
- Oxidative pathways successfully introduced functionalities at the C30 position.

## Abstract

Lupeol, a naturally occurring pentacyclic triterpenoid widely distributed in various medicinal plants, has attracted significant attention due to its diverse pharmacological properties. In this study, we report the synthesis and structural modification of 14 lupeol derivatives through selective functionalizations at C3 and C30 positions of the lupane skeleton, via the sequential chemoselective introduction of carbonyl moieties and the addition of organometallics. Emphasis has been given to the stereoselective alkylation at C3 using a range of carbanions, including organolithiums, organomagnesiums and organoindiums. The C30 position was modified through oxidative pathways to introduce several functionalities.