Cascade Cyclization of <i>N</i>-Cyanamide Alkenes for the Divergent Synthesis of Azido-, Nitro-, and Alkenyl-Containing Pyrroloquinazolinones

Radical cascade cyclizations of <i>N</i>-cyanamide alkenes have been developed for the divergent synthesis of pyrroloquinazolinones bearing azido, alkenyl, and nitro groups by controlling the reaction conditions. The reaction temperature and the loading of the base play important roles in the different reaction pathways. These reactions are characterized by wide functional group compatibility and mild conditions.

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Publication Details

Journal
Organic Letters
Published
2024-09-16
DOI
https://doi.org/10.1021/acs.orglett.4c02803
Citations
24
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
6.00

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article

Cascade Cyclization of N-Cyanamide Alkenes for the Divergent Synthesis of Azido-, Nitro-, and Alkenyl-Containing Pyrroloquinazolinones

Yun‐Tao Shen, Tai‐Gang Fan, Bo Jiang, Yu‐Song Ran et al.
24 citations
Organic Letters
Click Chemistry and Applications
6.00
article

Cascade Cyclization of N-Cyanamide Alkenes for the Divergent Synthesis of Azido-, Nitro-, and Alkenyl-Containing Pyrroloquinazolinones

Yun‐Tao Shen, Tai‐Gang Fan, Bo Jiang, Yu‐Song Ran, Ya‐Min Li, Cui Zhang, Yuan Qu
article en
24 citations

Abstract

Radical cascade cyclizations of <i>N</i>-cyanamide alkenes have been developed for the divergent synthesis of pyrroloquinazolinones bearing azido, alkenyl, and nitro groups by controlling the reaction conditions. The reaction temperature and the loading of the base play important roles in the different reaction pathways. These reactions are characterized by wide functional group compatibility and mild conditions.

Organic LettersVol. 26(38)
Kunming University of Science and Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 3%
Click Chemistry and Applications
6.00
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