Synthesis of benzo[b][1,4]oxazine adducts of c60 fullerene in the presence of lead(IV) acetate

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Дәйексөз келтіру

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Аннотация

A method was developed for the synthesis of fused benzo[b][1.4]oxazine monoadducts of С60 fullerene in reactions with aminophenols (2-aminophenol, 2-amino-4-methylphenol, 2-amino-4-phenylphenol) in the presence of LiOH and Pb(OAc)4. A probable mechanism for the reactions of obtaining condensed benzo[b][1,4]oxazine adducts has been proposed.

Авторлар туралы

Z. Kinzyabaeva

Institute of Petrochemistry and Catalysis

Email: zefa5@rambler.ru
Russia, 450075 Ufa, prosp. Oktyabrya, 141

Z. Fazletdinova

Institute of Petrochemistry and Catalysis

Russia, 450075 Ufa, prosp. Oktyabrya, 141

D. Sabirov

Institute of Petrochemistry and Catalysis

Russia, 450075 Ufa, prosp. Oktyabrya, 141

Әдебиет тізімі

  1. Трошин П.А., Любовская Р.Н. Усп. хим. 2008, 77, 323–369. [Troshin P.A., Lyubovskaya R.N., Russ. Chem. Rev. 2008, 77 (4), 305–349.] doi: 10.1070/RC2008v077n04ABEH003770]
  2. Handbook on Fullerene: Synthesis, Properties & Applications, Ed. R.F. Verner, C. Benvegnu, Hauppauge: Nova Science Pub Inc., UK, 2012, 548.
  3. Wang, G.-W., Yang H.-T., Miao C.-B., Xu, Y., Liu F. Org. Biomol. Chem. 2006, 4, 2595−2599. doi: 10.1039/B604626F
  4. Meier M.S., Poplawska M. Tetrahedron 1996, 52, 5043−5052. doi: 10.1016/0040-4020(96)00112-3
  5. Zhai W.-Q., Jiang S.-P., Peng R.-F., Jin B., Wang G.-W. Org. Lett. 2015, 17, 1862−1865. doi: 10.1021/acs.orglett.5b00536
  6. Kinzyabaeva Z.S., Sharipov G.L. Ultrason. Sonochem. 2018, 42, 119−123. doi: 10.1016/j.ultsonch.2017.11.012
  7. Delgado J.L., Cardinali F., Espíldora E., Torres M. R., Langa F., Martín N. Org. Lett. 2008, 10, 3705−3708. doi: 10.1021/ol801308g
  8. Li F.-B., Liu T.-X., Huang Y.-S., Wang G.-W. J. Org. Chem. 2009, 74, 7743−7749. doi: 10.1021/jo901028x
  9. Булгаков Р.Г., Кинзябаева З.С. ЖОрХ. 2014, 50, 1206−1210. [Bulgakov R.G., Kinzyabaeva Z.S. Russ. J. Org. Chem. 2014, 50, 1189−1193. doi: 10.1134/S107042801408020X]
  10. Chuang S.-C., Rajeshkumar V., Cheng C.-A., Deng J.-C., Wang G.-W. J. Org. Chem. 2011, 76, 1599−1604. doi: 10.1021/jo102107k
  11. Li F., Liu T.-X., Wang G.-W. Org. Lett. 2012, 14, 2176−2179. doi: 10.1021/ol3007452
  12. Yang H.-T., Liang X.-C., Wang Y.-H., Yang Y., Sun X.-Q., Miao C.-B. Org. Lett. 2013, 15, 4650−4653. doi: 10.1021/ol401909z
  13. You X., Wang G.-W. J. Org. Chem. 2014, 79, 117−121. doi: 10.1021/jo402354w
  14. Zhai W.-Q., Peng R.-F., Jin B., Wang G.-W. Org. Lett. 2014, 16, 1638−1641. doi: 10.1021/ol5002818
  15. Yang H.-T., Lu X.-W., Xing M.-L., Sun X.-Q., Miao C.-B. Org. Lett. 2014, 16, 5882−5885. doi: 10.1021/ol5028305
  16. Kinzyabaeva Z. S., Sabirov D. Sh. Ultrason. Sonochem. 2020, 67, 10569. doi: 10.1016/j.ultsonch.2020.105169
  17. Джемилев У.М., Ибрагимов А.Г., Туктаров А.Р., Пудас М., Валямова Ф.Г. А.С. 2006115735/04 (2006). РФ. Б.И. 2007, № 31.
  18. Zhen J., Liu Q., Chen X., Li D., Qiao Q., Lu Y., Yang S. J. Mater. Chem. A, 2016, 4, 8072–8079. doi: 10.1039/C6TA02016J
  19. Yang H.-T., Ge J., Lu X.-W., Sun X.-Q., Miao C.-B. J. Org. Chem. 2017, 82, 5873−5880. doi: 10.1021/acs.joc.7b00741
  20. Кинзябаева З.С., Шарипов Г.Л. А.С. 2020137553 (2020). РФ. Б.И. 2022, № 15.
  21. Kinzyabaeva Z.S., Sabirov D.Sh. Fullerenes, Nanotub. Carbon Nanostruct. 2022, 30, 1134–1141. doi: 10.1080/1536383X.2022.2078314
  22. Кинзябаева З.С., Сабиров Д.Ш. ЖОрХ. 2023, 59, 237–242. [Kinzyabaeva Z. S., SharipovG. L. Russ. J. Org. Chem. 2022, 58, 1915–1919. doi: 10.1134/s1070428022120223]. doi: 10.31857/S051474922302009X
  23. Кинзябаева З.С., Шарипов Г.Л. ЖОрХ. 2018, 54, 1102–1104. [Kinzyabaeva Z.S., Sharipov G.L. Russ. J. Org. Chem. 2018, 54, 1112–1115. doi: 10.1134/S1070428018070254]. doi: 10.7868/S0514749218070257
  24. Kinzyabaeva Z.S., Dmitriev A.M., Sabirov D.Sh. Fullerenes, Nanotub. Carbon Nanostruct. 2021, 29, 601−607. doi: 10.1080/1536383X.2021.1873782
  25. Кинзябаева З.С. ХГС 2021, 57 (5), 602–605. [Kinzyabaeva Z. S. Chem. Heterocycl. Compd. 2021, 57 (5), 602–605.] doi: 10.1007/s10593-021-02950-2
  26. Isaacs L., Wehrsig A., Diederich F. Helv. Chim. Acta. 1993, 76, 1231–1250. doi: 10.1002/hlca.19930760310
  27. Elemes Y., Silverman S.K., Sheu C., Kao M., Fo- ote C.S., Alvarez M.M., Whetten R.L. Angew. Chem., Int. Ed. Engl. 1992, 31, 351–353. doi: 10.1002/anie.199203511
  28. Hirsch A., Li Q., Wundl L., Wundl F. Angew. Chem. Int. Ed. Engl. 1991, 30, 1309–1310. doi: 10.1002/anie.199113091
  29. Wudl F., Hirsch A., Khemani K.C., Suzuki T., Allemand P.-M., Koch A., Eckert H., Srdanov G., Webb H.M. Fullerenes. Synthesis, Properties, and Chemsitry of Large Carbon Clusters, ACS Symposium Series, eds. G.S. Hammond, V.J. Kuck, Washington: American Chemical Society, 1992, 481, 161–175.
  30. Lobach A.S., Goldshleger N.F., Kaplunov M.G., Kulikov A.V. Chem. Phys. Lett. 1995, 243, 22–28. doi: 10.1016/0009-2614(95)00811-H
  31. Chuang S.-C., Clemente F.R., Khan S.I., Houk K.N., Rubin Y. Org. Lett. 2006, 8, 4525–4528. doi: 10.1021/ol061707e

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