Recent Synthetic Applications of Catalyst-Free Photochemistry

被引:58
|
作者
Liu, Wenbo
Li, Chao-Jun [1 ]
机构
[1] McGill Univ, Dept Chem, 801 Sherbrooke St W, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
photochemistry; catalyst-free; organic synthesis; green chemistry; ENANTIOSELECTIVE TOTAL-SYNTHESIS; ASYMMETRIC TOTAL-SYNTHESIS; 1ST TOTAL-SYNTHESIS; INTRAMOLECULAR 2+2 PHOTOCYCLOADDITIONS; PHOTOINDUCED RADICAL CYCLIZATION; PHOTO-FRIES REARRANGEMENT; METAL-FREE; VISIBLE-LIGHT; CHEMICAL-SYNTHESIS; ARYL HALIDES;
D O I
10.1055/s-0036-1590900
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Catalyst-free photochemistry provides numerous opportunities toward sustainable synthesis because catalyst separation can usually be avoided, which is consistent with green chemistry principles. Complementary to the well-reviewed photoredox chemistry, this review specifically summarizes the synthetic applications of photochemistry without external catalysts reported since 2000. The selected examples include both natural product synthesis and new methodology development. This review is arranged based on the type of chromophore. It is our hope that this review will inspire more synthetic chemists to embrace photochemistry into their research plans. 1Introduction 2Photochemistry of Olefins 2.1[2+2] Cycloaddition of Enones and Olefins 2.2Cycloaddition of Olefins without Carbonyl Groups 2.3 Z/E Isomerization 2.4Cyclization 2.5Others 3Photochemistry of C=O 3.1The Patern-Buchi Reaction 3.2The Yang Photoenolization 3.3The Norrish Type I Reaction 3.4The Norrish Type II Reaction 3.5Others 4Photochemistry of Nitrogen-Containing Functional Groups 5Photochemistry of Halogen-Containing Compounds 6Conclusion and Outlook
引用
收藏
页码:2714 / 2754
页数:41
相关论文
共 50 条
  • [31] Catalyst-free synthesis of acenaphthoindolopyrimidine derivatives
    Nahale Kakavand
    Mohammad Bayat
    Yadollah Bayat
    Molecular Diversity, 2023, 27 : 1785 - 1793
  • [32] Catalytic and catalyst-free diboration of alkynes
    Zhao, Fei
    Jia, Xiuwen
    Li, Pinyi
    Zhao, Jingwei
    Zhou, Yu
    Wang, Jiang
    Liu, Hong
    ORGANIC CHEMISTRY FRONTIERS, 2017, 4 (11): : 2235 - 2255
  • [33] Catalyst-free and Reprocessable Aromatic Polydithiourethanes
    Bo Yang
    HaiJun Feng
    TianTian Ni
    XiaoRui Zhou
    Tao Xie
    Ning Zheng
    Chinese Journal of Polymer Science, 2024, 42 (10) : 1435 - 1441
  • [34] A catalyst-free synthesis of α-aminophosphonates in glycerol
    Azizi, Kobra
    Karimi, Meghdad
    Heydari, Akbar
    TETRAHEDRON LETTERS, 2014, 55 (52) : 7236 - 7239
  • [35] Catalyst-free and solvent-free hydroboration of ketones
    Wang, Weifan
    Luo, Man
    Yao, Weiwei
    Ma, Mengtao
    Pullarkat, Sumod A.
    Xu, Li
    Leung, Pak-Hing
    NEW JOURNAL OF CHEMISTRY, 2019, 43 (27) : 10744 - 10749
  • [36] Catalyst-free and solvent-free hydroboration of aldehydes
    Stachowiak, Hanna
    Kazmierczak, Joanna
    Kucinski, Krzysztof
    Hreczycho, Grzegorz
    GREEN CHEMISTRY, 2018, 20 (08) : 1738 - 1742
  • [37] Catalyst-free and solvent-free hydroboration of alkynes
    Jaladi, Ashok Kumar
    Choi, Hyeon Seong
    An, Duk Keun
    NEW JOURNAL OF CHEMISTRY, 2020, 44 (32) : 13626 - 13632
  • [38] Catalyst-Free Synthesis of ZnO Nanowires on Oxidized Silicon Substrate for Gas Sensing Applications
    Behera, B.
    Chandra, S.
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2015, 15 (06) : 4534 - 4542
  • [39] Catalyst-free synthesis of carbon nanospheres for potential biomedical applications: waste to wealth approach
    Manaf, Shoriya Aruni Abdul
    Roy, Partha
    Sharma, Korada V.
    Ngaini, Zainab
    Malgras, Victor
    Aldalbahi, Ali
    Alshehri, Saad M.
    Yamauchi, Yusuke
    Hegde, Gurumurthy
    RSC ADVANCES, 2015, 5 (31) : 24528 - 24533
  • [40] A solvent- and catalyst-free tandem reaction: synthesis, and photophysical and biological applications of isoindoloquinazolinones
    Bera, Anirban
    Ali, Sk Asraf
    Manna, Susanta Kumar
    Ikbal, Mohammed
    Misra, Sandip
    Saha, Amit
    Samanta, Shubhankar
    NEW JOURNAL OF CHEMISTRY, 2020, 44 (11) : 4324 - 4331