电邮这篇文章 Direct cross-dehydrogenative С–N-coupling of phenanthridine with 1H-benzotriazole
- 作者: Akulov A.A1, Pershin A.A1, Kopchuk D.S1,2, Varaksin M.V1,2, Zyryanov G.V1,2, Chupakhin O.N1,2
-
隶属关系:
- Ural Federal University named after the first President of Russia B.N. Yeltsin
- I.Ya. Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch of the Russian Academy of Sciences
- 期: 卷 59, 编号 7 (2023)
- 页面: 961-966
- 栏目: Articles
- URL: https://modernonco.orscience.ru/0514-7492/article/view/666243
- DOI: https://doi.org/10.31857/S051474922307011X
- EDN: https://elibrary.ru/HTVHBX
- ID: 666243
如何引用文章
开放存取
##reader.subscriptionAccessGranted##
订阅存取
详细
An approach was developed for the direct C( sp 2)-H-functionalization of phenanthridine with a 1 H -benzotriazole residue, carried out in the presence of Selectfluor® reagent and leading to the formation of a C( sp 2)-N bond. The procedure described in this communication makes it possible to obtain α-(1 H -benzotriazol-1-yl)phenanthridine, which is a valuable synthon for further chemical transformations, in one step and using commercially available substrates and reagents.
作者简介
A. Akulov
Ural Federal University named after the first President of Russia B.N. Yeltsin
A. Pershin
Ural Federal University named after the first President of Russia B.N. Yeltsin
D. Kopchuk
Ural Federal University named after the first President of Russia B.N. Yeltsin;I.Ya. Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch of the Russian Academy of Sciences
M. Varaksin
Ural Federal University named after the first President of Russia B.N. Yeltsin;I.Ya. Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch of the Russian Academy of Sciences
G. Zyryanov
Ural Federal University named after the first President of Russia B.N. Yeltsin;I.Ya. Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch of the Russian Academy of Sciences
Email: gvzyryanov@gmail.com
O. Chupakhin
Ural Federal University named after the first President of Russia B.N. Yeltsin;I.Ya. Postovsky Institute of Organic Synthesis, Russian Academy of Sciences, Ural Branch of the Russian Academy of Sciences
参考
- Taniya O.S., Kopchuk D.S., Khasanov A.F., Kovalev S.I., Santra S., Zyryanov G.V., Majee A., Charushin V.N., Chupakhin O.N. Coord. Chem. Rev. 2021, 442, 213980. doi: 10.1016/j.ccr.2021.213980
- Tumir L.M., Radić Stojković M., Piantanida I. Beilstein J. Org. Chem. 2014, 10, 2930-2954. doi: 10.3762/bjoc.10.312
- Pipe D.F., Rees C.W. J. Chem. Soc., Chem. Commun. 1982, 9, 520-521. doi: 10.1039/C39820000520
- Houghton P.G., Pipe D.F., Rees C.W., J. Chem. Soc., Perkin Trans. 1. 1985, 1471-1479. doi: 10.1039/P19850001471
- Murakami K., Yamada S., Kaneda T., Itami K., Chem. Rev. 2017, 117, 9302-9332. doi: 10.1021/acs.chemrev.7b00021
- Mukherjee A., Akulov A.A., Santra S., Varaksin M.V., Kim G.A., Kopchuk D.S., Taniya O.S., Zyryanov G.V., Chupakhin O.N. RSC Adv. 2022, 12, 9323-9341. doi: 10.1039/d2ra00260d
- Taniya O.S., Khasanov A.F., Varaksin M.V., Starnovskaya E.S., Krinochkin A.P., Savchuk M.I., Kopchuk D.S., Kovalev I.S., Kim G.A., Nosova E.V., Zyryanov G.V., Chupakhin O.N. New J. Chem. 2021, 45, 20955-20971. doi: 10.1039/d1nj03531b
- Santra S., Khasanov A.F., Mukherjee A., Rahman M., Kovalev I.S., Kopchuk D.S., Zyryanov G.V., Majee A., Chupakhin O.N., Charushin V.N. Eur. J. Org. Chem. 2018, 2018, 4351-4375. doi: 10.1002/ejoc.201800635
- Taniya O.S., Kopchuk D.S., Khasanov A.F., Kovalev I.S., Santra S., Rahman M., Zyryanov G.V., Majee A., Charushin V.N., Chupakhin O.N. New J. Chem. 2019, 43, 11382-11390. doi: 10.1039/c9nj01813a
- Akulov A.A., Varaksin M.V., Tsmokalyuk A.N., Charushin V.N., Chupakhin O.N. Green Chem. 2021, 23, 2049-2057. doi: 10.1039/D1GC00175B
- Акулов А.А., Вараксин М.В., Чарушин В.Н., Чупахин О.Н. ХГС. 2019, 55, 783-787.
- Akulov A.A., Varaksin M.V., Charushin V.N., Chupakhin O.N. Chem. Heterocycl. Compd. 2019, 55, 783-787. doi: 10.1039/D1GC00175B
- Xie L.Y., Qu J., Peng S., Liu K.J., Wang Z., Ding M.H., Wang Y., Cao Z., He W.M. Green Chem. 2018, 20, 760-764. doi: 10.1039/c7gc03106h
- Morgan G.T., Walls L.P. J. Chem. Soc. 1932, 2225-2231. doi: 10.1039/JR9320002225
- Parenty A.D.C., Smith L.V., Pickering A.L., Long D.-L., Cronin L. J. Org. Chem. 2004, 69, 5934-5946. doi: 10.1021/jo0495440
- Couturier M., Caron L., Tumidajski S., Jones K., White T.D. Org. Lett. 2006, 8, 1929-1932. doi: 10.1021/ol060473w
- Kim D., Ghosh P., Kwon N.Y., Han S.H., Han S., Mishra N.K., Kim S., Kim I.S. J. Org. Chem. 2020, 85, 2476-2485. doi: 10.1021/acs.joc.9b03173
- Yan L., Zhao D., Lan J., Cheng Y., Guo Q., Li X., Wu N., You J. Org. Biomol. Chem. 2013, 11, 7966-7977. doi: 10.1039/C3OB41760C
补充文件
