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Spin States Matter─from Fundamentals toward Synthetic Methodology Development and Drug Discovery
Accounts of Chemical Research ( IF 16.4 ) Pub Date : 2024-09-02 , DOI: 10.1021/acs.accounts.4c00405 Claire Empel 1 , Quoc Hoang Pham 1 , Rene M Koenigs 1
Accounts of Chemical Research ( IF 16.4 ) Pub Date : 2024-09-02 , DOI: 10.1021/acs.accounts.4c00405 Claire Empel 1 , Quoc Hoang Pham 1 , Rene M Koenigs 1
Affiliation
The potent reactivity of carbenes and nitrenes has been traditionally harnessed by the employment of a transition-metal catalyst in which the reactivity of the metal carbene/nitrene intermediates can be controlled via the judicious tuning of the metal catalyst. In recent years, progress made in this research area has unveiled novel strategies to directly access free carbenes or nitrenes under visible-light-mediated conditions without the necessity of a metal catalyst for stabilization of the carbene/nitrene intermediate. Such photochemical approaches present new opportunities to leverage orthogonal reactions with classic metal-catalyzed transformations.
中文翻译:
自旋态很重要——从基础知识到合成方法开发和药物发现
传统上,通过使用过渡金属催化剂来利用卡宾和氮宾的有效反应性,其中金属卡宾/氮宾中间体的反应性可以通过金属催化剂的明智调节来控制。近年来,该研究领域取得的进展揭示了在可见光介导条件下直接获取游离卡宾或氮宾的新策略,而无需金属催化剂来稳定卡宾/氮宾中间体。这种光化学方法提供了利用正交反应与经典金属催化转化的新机会。
更新日期:2024-09-02
中文翻译:
自旋态很重要——从基础知识到合成方法开发和药物发现
传统上,通过使用过渡金属催化剂来利用卡宾和氮宾的有效反应性,其中金属卡宾/氮宾中间体的反应性可以通过金属催化剂的明智调节来控制。近年来,该研究领域取得的进展揭示了在可见光介导条件下直接获取游离卡宾或氮宾的新策略,而无需金属催化剂来稳定卡宾/氮宾中间体。这种光化学方法提供了利用正交反应与经典金属催化转化的新机会。