# α-Carbonyl Rh-Carbenoid Initiated Cascade Assembly of Diazobarbiturates with Alkylidene Pyrazolones for Synthesis of Spirofuropyrimidines

**Authors:** Yue Zhang, Yu-Hang Mi, Kuo Wang, Hong-Wu Zhao

PMC · DOI: 10.3390/molecules29133178 · Molecules · 2024-07-03

## TL;DR

A rhodium-catalyzed reaction efficiently produces spirofuropyrimidines from diazobarbiturates and alkylidene pyrazolones.

## Contribution

A new cascade assembly method for synthesizing spirofuropyrimidines using Rh2(esp)2 and BINAP catalysts.

## Key findings

- The reaction achieved 38–96% yields of spirofuropyrimidines under optimized conditions.
- X-ray diffraction confirmed the chemical structure of the synthesized compounds.

## Abstract

Catalyzed by Rh2(esp)2 (10 mol%) and (±)-BINAP (20 mol%) in DCE at 80 °C, the cascade assembly between diazobarbiturates and alkylidene pyrazolones proceeded readily and produced spiro-furopyrimidines in 38–96% chemical yields. The chemical structure of the prepared spirofuro-pyrimidines was firmly confirmed by X-ray diffraction analysis.

## Linked entities

- **Chemicals:** Rh2(esp)2 (PubChem CID 16218143), BINAP (PubChem CID 634876)

## Full-text entities

- **Chemicals:** Alkylidene Pyrazolones (-), (+-)-BINAP (MESH:C406943)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11243257/full.md

## References

82 references — full list in the complete paper: https://tomesphere.com/paper/PMC11243257/full.md

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Source: https://tomesphere.com/paper/PMC11243257