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Russian Chemical Reviews, 1974, Volume 43, Issue 8, Pages 679–689
DOI: https://doi.org/10.1070/RC1974v043n08ABEH001845
(Mi rcr2733)
 

This article is cited in 88 scientific papers (total in 88 papers)

The Ullmann Ether Condensation

A. A. Moroza, M. S. Shvartsbergb

a Novosibirsk State University
b Institute of Chemical Kinetics and Combustion, Siberian Branch of the USSR Academy of Sciences, Novosibirsk
Abstract: The review deals with the Ullmann condensation as the most important method for the synthesis of aromatic ethers. The available information about the dependence of the reactivity of the reactants on structure and the reaction mechanism is examined and the experimental condensation conditions are discussed.
The bibliography includes 241 references.
Bibliographic databases:
Document Type: Article
UDC: 547.211+547.223+547.322
Language: English
Original paper language: Russian


Citation: A. A. Moroz, M. S. Shvartsberg, “The Ullmann Ether Condensation”, Usp. Khim., 43:8 (1974), 1443–1461; Russian Chem. Reviews, 43:8 (1974), 679–689
Linking options:
  • https://www.mathnet.ru/eng/rcr2733
  • https://doi.org/10.1070/RC1974v043n08ABEH001845
  • https://www.mathnet.ru/eng/rcr/v43/i8/p1443
  • This publication is cited in the following 88 articles:
    1. Shurutishria Ramakrishnan, Sakunthala Paramewaran, Nadiah Mad Nasir, Chem. Pap., 75:2 (2021), 455  crossref
    2. Susanta Banerjee, Debaditya Bera, Membrane Materials for Gas and Vapor Separation, 2017, 223  crossref
    3. Xiantao Ma, Quan Liu, Xiaojuan Jia, Chenliang Su, Qing Xu, RSC Adv., 6:62 (2016), 56930  crossref
    4. Simon Sung, David Sale, D. Christopher Braddock, Alan Armstrong, Colin Brennan, Robert P. Davies, ACS Catal., 6:6 (2016), 3965  crossref
    5. Guang-Lin Song, Zhang Zhang, Yu-Xia Da, Xi-Cun Wang, Tetrahedron, 71:46 (2015), 8823  crossref
    6. Sipra Ghosh, Rajdeep Mukherjee, Anindita Ghosh, Aruna Kumar Mohanty, Susanta Banerjee, Handbook of Specialty Fluorinated Polymers, 2015, 11  crossref
    7. Baghbanian S.M., Yadollahy H., Tajbakhsh M., Farhang M., Biparva P., RSC Adv., 4:107 (2014), 62532–62543  crossref  isi
    8. Debasish Kundu, Pintu Maity, Brindaban C. Ranu, Org. Lett., 16:4 (2014), 1040  crossref
    9. Fangliang Liu, Huameng Yang, Xinquan Hu, Gaoxi Jiang, Org. Lett., 16:24 (2014), 6408  crossref
    10. Corinne Vanucci-Bacqué, Slim Chaabouni, Isabelle Fabing, Florence Bedos-Belval, Michel Baltas, Tetrahedron Letters, 55:2 (2014), 528  crossref
    11. S. Quideau, D. Deffieux, L. Pouységu, Comprehensive Organic Synthesis II, 2014, 656  crossref
    12. Noriaki Takemura, Yoichiro Kuninobu, Motomu Kanai, Org. Biomol. Chem., 12:16 (2014), 2528  crossref
    13. B. G. Jadhav, S. D. Samant, Russ J Org Chem, 50:9 (2014), 1301  crossref
    14. Waszkielewicz A.M., Gunia A., Szkaradek N., Pytka K., Siwek A., Satala G., Bojarski A.J., Szneler E., Marona H., Bioorg. Med. Chem. Lett., 23:15 (2013), 4419–4423  crossref  isi
    15. Natalia Szkaradek, Agnieszka Gunia, Anna M. Waszkielewicz, Lucyna Antkiewicz-Michaluk, Marek Cegła, Edward Szneler, Henryk Marona, Bioorganic & Medicinal Chemistry, 21:5 (2013), 1190  crossref
    16. Shafeek A. R. Mulla, Suleman M. Inamdar, Mohsinkhan Y. Pathan, Santosh S. Chavan, RSC Adv., 2:33 (2012), 12818  crossref
    17. Kye-Simeon Masters, Stefan Bräse, Chem. Rev., 112:7 (2012), 3717  crossref
    18. Shafeek A.R. Mulla, Suleman M. Inamdar, Mohsinkhan Y. Pathan, Santosh S. Chavan, Tetrahedron Letters, 53:14 (2012), 1826  crossref
    19. Ze He, Chi-Wai Kan, Cheuk-Lam Ho, Wai-Yeung Wong, Chung-Hin Chui, Ka-Lap Tong, Shu-Kong So, Tik-Ho Lee, Louis M. Leung, Zhenyang Lin, Dyes and Pigments, 88:3 (2011), 333  crossref
    20. Rongzhao Zhang, Jianming Liu, Shoufeng Wang, Jianzhong Niu, Chungu Xia, Wei Sun, ChemCatChem, 3:1 (2011), 146  crossref
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