# Synthetic study toward vibralactone

**Authors:** Liang Shi, Jiayi Song, Yiqing Li, Jia-Chen Li, Shuqi Li, Li Ren, Zhi-Yun Liu, Hong-Dong Hao

PMC · DOI: 10.3762/bjoc.21.182 · Beilstein Journal of Organic Chemistry · 2025-11-04

## TL;DR

This paper describes a new synthetic approach to create vibralactone, a compound that inhibits pancreatic lipase.

## Contribution

A novel method for synthesizing an all-carbon quaternary center in vibralactone is introduced.

## Key findings

- The all-carbon quaternary center in vibralactone was successfully synthesized.
- Intramolecular alkylidene carbene C–H insertion was used to form the cyclopentene ring.

## Abstract

A synthetic study toward vibralactone, a potent inhibitor of pancreatic lipase, is reported. The synthesis of the challenging all-carbon quaternary center within the cyclopentene ring was achieved through intramolecular alkylidene carbene C–H insertion.

## Linked entities

- **Chemicals:** vibralactone (PubChem CID 16095274)

## Full-text entities

- **Genes:** PNLIP (pancreatic lipase) [NCBI Gene 5406] {aka PL, PNLIPD, PTL}
- **Chemicals:** cyclopentene (MESH:D003517), vibralactone (MESH:C522315), carbon (MESH:D002244), alkylidene carbene (-)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12599391/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12599391/full.md

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Source: https://tomesphere.com/paper/PMC12599391