Cu-Catalyzed Relay Functionalization of Alkenes: Diverse Synthesis of Diazidated Quinazolinones and Polycyclic Imidazoles

A Cu-catalyzed relay process for the preparation of diazidated quinazolinone and polycyclic imidazole derivatives in which readily available alkene-tethered substrates undergo an addition/cyclization/C(sp<sup>3</sup>)-H functionalization of alkene sequences with high efficiency is described. Various functionalized N-heteropolycyclic compounds were readily prepared in good yields with a broad substrate scope. Moreover, the direct azidation of the α-C(sp<sup>3</sup>)-H bond of the corresponding N-heterocycles has been demonstrated on the basis of mechanistic studies, which provide an alternative late-stage functionalization approach for the derivatization of N-heterocyclic scaffolds.

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Publication Details

Journal
Organic Letters
Published
2025-01-09
DOI
https://doi.org/10.1021/acs.orglett.4c04353
Citations
11
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
10.30

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article

Cu-Catalyzed Relay Functionalization of Alkenes: Diverse Synthesis of Diazidated Quinazolinones and Polycyclic Imidazoles

Zhonglin Wei, Ji-Ming Xi, Wei‐Wei Liao
11 citations
Organic Letters
Catalytic C–H Functionalization Methods
10.30
article

Cu-Catalyzed Relay Functionalization of Alkenes: Diverse Synthesis of Diazidated Quinazolinones and Polycyclic Imidazoles

Zhonglin Wei, Ji-Ming Xi, Wei‐Wei Liao
article en
11 citations

Abstract

A Cu-catalyzed relay process for the preparation of diazidated quinazolinone and polycyclic imidazole derivatives in which readily available alkene-tethered substrates undergo an addition/cyclization/C(sp<sup>3</sup>)-H functionalization of alkene sequences with high efficiency is described. Various functionalized N-heteropolycyclic compounds were readily prepared in good yields with a broad substrate scope. Moreover, the direct azidation of the α-C(sp<sup>3</sup>)-H bond of the corresponding N-heterocycles has been demonstrated on the basis of mechanistic studies, which provide an alternative late-stage functionalization approach for the derivatization of N-heterocyclic scaffolds.

Organic LettersVol. 27(3)
Jilin University (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN)
State Key Laboratory of Supramolecular Structure and Materials
Openalex Percentile: Top 2%
Catalytic C–H Functionalization Methods
10.30
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Cu-Catalyzed Relay Functionalization of Alkenes: Diverse Synthesis of Diazidated Quinazolinones and Polycyclic Imidazoles — Zhonglin Wei, Ji-Ming Xi, et al. · Organic Letters (2025) | TGRS Research Map | TGRS