Журнал "Макрогетероциклы"

1. Balzani V., Credi A., Venturi M. Molecular Devices and Machines – Concepts and Perspectives for the Nanoworld. Weinheim: Wiley - VCH, 2008. 546 p.

 

2. Molecular Switches (Feringa B.L., Browne W.R., Eds.) Weinheim: Wiley - VCH, 2011. 824 p.

 

3. Antipin I.S., Kazymova M.A., Kuznetsov M.A., Vasilyev A.V., Ishchenko M.A., Kiryushkin A.A., Kuznetsov L.M., Makarenko S.V., Ostrovskii V.A., Petrov M.L., Solod O.V., Trishin Yu.G., Yakovlev I.P., Nenaidenko V.G., Beloglazkinai E.K., Beletskaya I.P., Ustynyuk Yu.A., Solov'ev P.A., Ivanov I.V., Malina E.V., Sivova N.V., Negrebetskii V.V., Baukov Yu.I., Pozharskaya N.A., Traven' V.F., Shchekotikhin A.E., Varlamov A.V., Borisova T.N., Lesina Yu.A., Krasnokutskaya E.A., Rogozhnikov S.I., Shurov S.N., Kustova T.P., Klyuev M.V., Khelevina O.G., Stuzhin P.A., Fedorov A.Yu., Gushchin A.V., Dodonov V.A., Kolobov A.V., Plakhtinskii V.V., Orlov V.Yu., Kriven'ko A.P., Fedotova O.V., Pchelintseva N.V., Charushin V.N., Chupakhin O.N., Klimochkin Yu.N., Klimochkina A.Yu., Kuryatnikov V.N., Malinovskaya Yu.A., Levina A.S., Zhuravleva O.E., Voronchikhina L.I., Fisyuk A.S., Aksenov A.V., Aksenova N.A., Aksenov I.V. Russ. J. Org. Chem. 2017, 53, 1275–1437.
https://doi.org/10.1134/S1070428017090019

 

4. Balzani V., Credi A., Venturi M. Chem. Soc. Rev. 2009, 38, 1542–1550.
https://doi.org/10.1039/b806328c

 

5. Qu D.-H., Wang Q.-Ch., Zhang Q.-W., Ma X., Tian H. Chem. Rev. 2015, 115, 7543–7588.
https://doi.org/10.1021/cr5006342

 

6. Calixarenes and Beyond (Neri P., Sessler J.L., Wang M.-X., Eds.) Netherlands: Springer, 2016. 1062 p.

 

7. Solovieva S.E., Burilov V.A., Antipin I.S. Macroheterocycles 2017, 10, 134–146.
https://doi.org/10.6060/mhc170512a

 

8. Konovalov A.I., Antipin I.S. Mendeleev Commun. 2008, 18, 229–237.
https://doi.org/10.1016/j.mencom.2008.09.001

 

9. Kumar R., Lee Y.O., Bhalla V., Kumar M., Kim J.S. Chem. Soc. Rev. 2014, 43, 4824–4870.
https://doi.org/10.1039/c4cs00068d

 

10. Burilov V.A., Mironova D.A., Ibragimova R.R., Solovieva S.E., Antipin I.S., König B. RSC Adv. 2015, 5, 101177–101185.
https://doi.org/10.1039/C5RA18294H

 

11. Jie K., Zhou Y., Yao Y., Huang F. Chem. Soc. Rev. 2015, 44, 3568–3587.
https://doi.org/10.1039/C4CS00390J

 

12. Burilov V.A., Mironova D.A., Ibragimova R.R., Nugmanov R.I., Solovieva S.E., Antipin I.S. Colloids Surf., A: Physicochem. Eng. Aspects 2017, 515, 41–49.
https://doi.org/10.1016/j.colsurfa.2016.12.007

 

13. Ovsyannikov A., Solovieva S., Antipin I., Ferlay S. Coord. Chem. Rev. 2017, 352, 151–186.
https://doi.org/10.1016/j.ccr.2017.09.004

 

14. Zhang H., Zou R., Zhao Y. Coord. Chem. Rev. 2015, 292, 74–90.
https://doi.org/10.1016/j.ccr.2015.02.012

 

15. Ovsyannikov A.S., Ferlay S., Solovieva S.E., Antipin I.S., Konovalov A.I., Kyritsakas N., Hosseini M.W. Macroheterocycles 2017, 10, 147–153.
https://doi.org/10.6060/mhc170295o

 

16. Yushkova E.A., Zaikov E.N., Stoikov I.I., Antipin I.S. Russ. Chem. Bull. Int. Ed. 2009, 58, 101–107.

 

17. Shao L., Hua B., Yang J., Yu G. Chem. Commun. 2016, 52, 6573–6576.
https://doi.org/10.1039/C6CC02434C

 

18. Armarego W.L.F., Chai C.L.L. Purification of Laboratory Chemicals. New York: Elsevier, 2009. 760 p.

 

19. Iki N., Kabuto C., Fukushima T., Kumagai H., Takeya H., Miyanari S., Miyashi T., Miyano S. Tetrahedron 2000, 56, 1437–1443.
https://doi.org/10.1016/S0040-4020(00)00030-2

 

20. Mokhtari B., Pourabdollah K., Dalaliy N. J. Coord. Chem. 2011, 64, 743–794.
https://doi.org/10.1080/00958972.2011.555538