One-Pot Total Synthesis of Natural Products Nitramarine, Nitraridine, and Analogues via a Cascade Oxidation/Pictet–Spengler Condensation/Annulation Process

A cascade oxidation/Pictet-Spengler condensation/annulation process has been developed for the one-pot total synthesis of nitramarine, nitraridine, and their analogues. The procedure proceeded with easily available quinolines and tryptophan derivatives. A simple and metal-free approach, wide substrate scope, and functional group tolerance make it applicable for the synthesis of diverse bioactive nitramarine, nitraridine, and their derivatives. Furthermore, the bioactivity evaluation has identified two promising leading compounds <b>5d</b> and <b>5e</b> with potent antitumor proliferative activity against breast cancer cells.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-08-09
DOI
https://doi.org/10.1021/acs.joc.4c01441
Citations
9
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.25

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article

One-Pot Total Synthesis of Natural Products Nitramarine, Nitraridine, and Analogues via a Cascade Oxidation/Pictet–Spengler Condensation/Annulation Process

An‐Xin Wu, Ming‐Xuan Wang, Yanping Zhu, Wenhui Cao et al.
9 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
2.25
article

One-Pot Total Synthesis of Natural Products Nitramarine, Nitraridine, and Analogues via a Cascade Oxidation/Pictet–Spengler Condensation/Annulation Process

An‐Xin Wu, Ming‐Xuan Wang, Yanping Zhu, Wenhui Cao, Yuanyuan Sun, Runqing Wang, Song Yingchun
article en
9 citations

Abstract

A cascade oxidation/Pictet-Spengler condensation/annulation process has been developed for the one-pot total synthesis of nitramarine, nitraridine, and their analogues. The procedure proceeded with easily available quinolines and tryptophan derivatives. A simple and metal-free approach, wide substrate scope, and functional group tolerance make it applicable for the synthesis of diverse bioactive nitramarine, nitraridine, and their derivatives. Furthermore, the bioactivity evaluation has identified two promising leading compounds <b>5d</b> and <b>5e</b> with potent antitumor proliferative activity against breast cancer cells.

The Journal of Organic ChemistryVol. 89(17)
Yantai University (CN), Central China Normal University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 12%
Catalytic C–H Functionalization Methods
2.25
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