# Melifoliox B, a novel phloroglucin derivative isolated from Melicope barbigera (Rutaceae) and synthesis of new oxidation products from melifoliones A and B

**Authors:** Horst Weber, Kim-Thao Tran-Cong, Bernhard Mayer, Guido J Reiss, Iryna S Konovalova, Marc S Appelhans, Kenneth R Wood, Claus M Passreiter

PMC · DOI: 10.3762/bjoc.22.39 · Beilstein Journal of Organic Chemistry · 2026-03-24

## TL;DR

Scientists isolated and synthesized new compounds from a plant, discovering novel ring structures not previously known.

## Contribution

The discovery of new heterocyclic ring systems formed through oxidative ring contraction, not previously described in the literature.

## Key findings

- Oxidation of melifoliones failed to produce expected products but yielded unexpected derivatives like 8, 9, and 10.
- Combined oxidation with hydrogen peroxide and ferricyanide formed novel furanone ring derivatives 11 and 12.
- X-ray analysis confirmed the structures of derivatives 11 and 12, representing new ring systems.

## Abstract

In addition to new acetophenones and 2H-chromenes, the dichlormethane extract from leaves of Melicope barbigera A. Gray (Rutaceae) afforded a mixture of the isomeric melifoliones A (1) and B (2) as well as an oxidation product of 2, whose structure was elucidated as the para-quinol 4. For an independent synthesis of 4 and its possible isomer 3, the required compounds 1 and 2 were synthesized as a mixture of the isomers starting from chromene 5, briefly heated in a closed microwave apparatus with catalytic amounts of acetic acid. Forced heating of 5 in acetic acid or use of stronger acids lead to the benzoxocin derivatives 6 and 7. Oxidation of melifoliones 1 and 2 under a great variety of oxidants and conditions failed to give 3 and 4. Iodine-containing oxidants yielded the products 8, 9, and 10. Combined oxidation with hydrogen peroxide and ferricyanide in alkaline solution resulted in an unexpected contraction of the acetyl phenol to a furanone ring, forming the derivatives 11 and 12, whose structures were confirmed by X-ray analysis. A hypothetical mechanism for the oxidative ring contraction is proposed. 11 and 12 are the first representatives of new heterocyclic ring systems that have not previously been described in the literature.

## Linked entities

- **Chemicals:** acetic acid (PubChem CID 176), hydrogen peroxide (PubChem CID 784), ferricyanide (PubChem CID 439210), iodine (PubChem CID 807)
- **Species:** Melicope barbigera (taxon 1336615)

## Full-text entities

- **Chemicals:** ferricyanide (MESH:C007931), phloroglucin (MESH:D010696), Iodine (MESH:D007455), benzoxocin derivatives 6 and 7 (-), acetyl phenol (MESH:C025136), B (MESH:D001895), acetic acid (MESH:D019342), hydrogen peroxide (MESH:D006861), acetophenones (MESH:D000098), 2H-chromenes (MESH:C412074)
- **Species:** Melicope barbigera (species) [taxon 1336615]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13040265/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC13040265/full.md

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Source: https://tomesphere.com/paper/PMC13040265