Cu(II)-Catalyzed Reaction of Ethynyl Methylene Cyclic Carbamates and Amines: Synthesis of Polysubstituted Pyrroles

A copper-catalyzed efficient, operationally simple, general method for straightforward syntheses of polysubstituted pyrroles employing ethynyl methylene cyclic carbamates as precursors reacting with commercially available amines was first reported. A wide variety of polysubstituted pyrroles were obtained in acceptable to good yields under mild conditions. This protocol features broad substrate scope, high functional group tolerance, and easy operation, therefore enabling late-stage functionalization and rapid synthesis of bioactive compounds, including structurally complex marketed drugs and natural products. In addition, a scale-up experiment further highlighted the synthetic utility.

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Publication Details

Journal
Organic Letters
Published
2024-10-18
DOI
https://doi.org/10.1021/acs.orglett.4c03334
Citations
9
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
Field-Weighted Citation Impact
2.25

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article

Cu(II)-Catalyzed Reaction of Ethynyl Methylene Cyclic Carbamates and Amines: Synthesis of Polysubstituted Pyrroles

Yujie Zhao, Liangjian Hu, Shijie Zhu, Shiwu Li et al.
9 citations
Organic Letters
Synthesis and Characterization of Pyrroles
2.25
article

Cu(II)-Catalyzed Reaction of Ethynyl Methylene Cyclic Carbamates and Amines: Synthesis of Polysubstituted Pyrroles

Yujie Zhao, Liangjian Hu, Shijie Zhu, Shiwu Li, Zhifei Zhao
article en
9 citations

Abstract

A copper-catalyzed efficient, operationally simple, general method for straightforward syntheses of polysubstituted pyrroles employing ethynyl methylene cyclic carbamates as precursors reacting with commercially available amines was first reported. A wide variety of polysubstituted pyrroles were obtained in acceptable to good yields under mild conditions. This protocol features broad substrate scope, high functional group tolerance, and easy operation, therefore enabling late-stage functionalization and rapid synthesis of bioactive compounds, including structurally complex marketed drugs and natural products. In addition, a scale-up experiment further highlighted the synthetic utility.

Organic LettersVol. 26(43)
Shihezi University (CN), Centre National de la Recherche Scientifique (FR), Université Paris-Saclay (FR), Institut de Chimie Moléculaire et des Matériaux d'Orsay (FR)
National Natural Science Foundation of China, Shihezi University
Clean water and sanitation
Openalex Percentile: Top 12%
Synthesis and Characterization of Pyrroles
2.25
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Cu(II)-Catalyzed Reaction of Ethynyl Methylene Cyclic Carbamates and Amines: Synthesis of Polysubstituted Pyrroles — Yujie Zhao, Liangjian Hu, et al. · Organic Letters (2024) | TGRS Research Map | TGRS