I<sub>2</sub>-DMSO mediated multi-component cascade cyclization to construct pyrazolo[3,4-<i>b</i>]pyrrolo[3,4-<i>d</i>]pyridine-6-one skeleton

A one-pot synthesis of the pyrazolo[3,4-<i>b</i>]pyrrolo[3,4-<i>d</i>]pyridin-6-one skeleton has been developed using aryl methyl ketones, 3-aminopyrazoles, and enaminamides as substrates. This method features metal-free catalysis and broad substrate compatibility (36 examples). The reaction involves the formation of two C-C and two C-N bonds, while constructing a tetrasubstituted carbon stereocenter bearing a reactive hydroxyl group.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra04871k
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.00

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article

I2-DMSO mediated multi-component cascade cyclization to construct pyrazolo[3,4-b]pyrrolo[3,4-d]pyridine-6-one skeleton

Ying Song, You Zhou, An‐Xin Wu, Yong‐Xing Tang et al.
RSC Advances
Synthesis and Reactivity of Heterocycles
article

I2-DMSO mediated multi-component cascade cyclization to construct pyrazolo[3,4-b]pyrrolo[3,4-d]pyridine-6-one skeleton

Ying Song, You Zhou, An‐Xin Wu, Yong‐Xing Tang, Lisheng Wang, Chun‐Yan Wu, Yan‐Dong Wu
article en

Abstract

A one-pot synthesis of the pyrazolo[3,4-<i>b</i>]pyrrolo[3,4-<i>d</i>]pyridin-6-one skeleton has been developed using aryl methyl ketones, 3-aminopyrazoles, and enaminamides as substrates. This method features metal-free catalysis and broad substrate compatibility (36 examples). The reaction involves the formation of two C-C and two C-N bonds, while constructing a tetrasubstituted carbon stereocenter bearing a reactive hydroxyl group.

RSC AdvancesVol. 15(34)
Central China Normal University (CN), Lanzhou University (CN)
National Natural Science Foundation of China, Higher Education Discipline Innovation Project
Openalex Percentile: Top 84%
Synthesis and Reactivity of Heterocycles
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