Quinazoline Synthesis via Rh(III)-Catalyzed Intermolecular C–H Functionalization of Benzimidates with Dioxazolones
收藏Figshare2016-05-02 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Quinazoline_Synthesis_via_Rh_III_Catalyzed_Intermolecular_C_H_Functionalization_of_Benzimidates_with_Dioxazolones/3166999
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An efficient double C–N bond formation sequence to prepare highly substituted quinazolines utilizing benzimidates and dioxazolones under the catalytic redox-neutral [Cp*RhCl2]2/AgBF4 system, where dioxazolones could work as an internal oxidant to maintain the catalytic cycle, is reported. N-Unsubstituted imine not only acts as a directing group but also functions as a nucleophile in postcoupling cyclization, and dioxazolone acts as a coupling partner for access to heterocycle.
创建时间：
2016-05-02
