Reductive Umpolung of Carbonyl Derivatives with Visible-Light Photoredox Catalysis: Direct Access to Vicinal Diamines and Amino Alcohols via α-Amino Radicals and Ketyl Radicals.

Reductive Umpolung of Carbonyl Derivatives with Visible-Light Photoredox Catalysis: Direct Access to Vicinal Diamines and Amino Alcohols via α-Amino Radicals and Ketyl Radicals.
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DOI:
10.1002/anie.201511235
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发表时间:
2016-06-01
影响因子:
16.6
通讯作者:
Rueping, Magnus
Rueping, Magnus
中科院分区:
化学1区
文献类型:
--
作者:
Fava, Eleonora;Millet, Anthony;Nakajima, Masaki;Loescher, Sebastian;Rueping, Magnus

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实现了可见光介导的光氧化还原催化醛亚胺-苯胺和醛亚胺-苯胺偶联。各种羰基衍生物的还原性单电子转移(SET)使中间体酮基和α-氨基自由基阴离子的产生成为可能,它们被用于合成不对称取代的1,2-二胺和氨基醇。
Visible‐light‐mediated photoredox‐catalyzed aldimine–aniline and aldehyde–aniline couplings have been realized. The reductive single electron transfer (SET) umpolung of various carbonyl derivatives enabled the generation of intermediary ketyl and α‐amino radical anions, which were utilized for the synthesis of unsymmetrically substituted 1,2‐diamines and amino alcohols.
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