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Photoredox Catalysis in Organophosphorus Chemistry

期刊

ASIAN JOURNAL OF ORGANIC CHEMISTRY
卷 6, 期 4, 页码 350-367

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.201600512

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资金

  1. Foundation Research Project of Jiangsu Province (The Natural Science Fund) [BK20141359]
  2. Fundamental Research Funds for the Central Universities [KYTZ201604]
  3. Beijing National Laboratory for Molecular Sciences (BNLMS)

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The vernal blooming of green chemistry has contributed to the development of visible light catalysis. Active radical species are generated from catalytic amounts of photosensitizers, such as transition-metal complexes and organic dyes, upon visible light irradiation. Stoichiometric amounts of oxidants, reductants, and radical initiators are avoided in most cases. Thus, reactions proceed under milder conditions with a broader functional group tolerance than found by other methods. Photoredox catalysis has been used to form C-C and C-X (X= O, N, and S) bonds but is comparably underdeveloped in organophosphorus chemistry. Herein, we summarize advances in photoredox catalysis that involve organophosphorus chemistry. The synthesis of organophosphorus compounds by photoredox catalysis, transition-metal complex/photoredox dual catalytic systems, and photoredox catalysis with phosphorus organocatalysts are discussed. The shortcomings and possible future trends of this chemistry are also presented.

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