Журнал "Макрогетероциклы"

1. a) Bridel M., Lavieille R. J. Pharm. Chim. 1931, 14, 369-379;
b) Mosettig E., Nes W.R. J. Org. Chem. 1955, 20, 884-899;
http://dx.doi.org/10.1021/jo01125a013
c) Rodrigues A.M.G.D., Lechat J.R. Acta Crystall. Sect. C 1988, 44, 1963-1965;
http://dx.doi.org/10.1107/S0108270188007279
d) Dolder F., Lichti H., Mosettig E., Quitt P. J. Am. Chem. Soc. 1960, 82, 246-247;
http://dx.doi.org/10.1021/ja01486a054
e) Waters J.A., Becker E.D., Mosettig E. J. Org. Chem. 1962, 27, 4689-4691;
http://dx.doi.org/10.1021/jo01059a533
f) Coates R.M., Bertram E.F. J. Org. Chem. 1971, 36, 2625-2631;
http://dx.doi.org/10.1021/jo00817a014
g) Coates R.M., Kang H.-Y. J. Org. Chem. 1987, 52, 2065-2074;
http://dx.doi.org/10.1021/jo00386a031
h) Hershenhorn J., Zohar M., Crammer B., Ziv Z., Weinstein V., Kleifeld Y., Lavan Y., Ikan R. Plant Growth Regul. 1997, 23, 173-178;
http://dx.doi.org/10.1023/A:1005934109197
i) Ikeda T., Kajimoto T., Kondo H., Wong C.-H. Bioorg. Med. Chem. Lett. 1997, 7, 2485-2490.
http://dx.doi.org/10.1016/S0960-894X(97)10022-1

 

2. a) Kataev V.E., Khaybullin R.N., Sharipova R.R., Strobykina I.Yu. Rev. J. Chem. 2011, 1, 93-160;
http://dx.doi.org/10.1134/S2079978011010043
b) Moons N., Borggraeve W.De, Dehaen W. Curr. Org. Chem. 2011, 15, 2731-2741;
http://dx.doi.org/10.2174/138527211796367372
c) Lohoelter Ch., Weckbecker M., Siegfried R. W. Eur. J. Org. Chem. 2013, 25, 5539-5554.
http://dx.doi.org/10.1002/ejoc.201300447

 

3. a) Ukiya M., Sawada Sh., Kikuchi T., Kushi Y., Fukatsu M., Akihisa T. Chem. Biodiversity. 2013, 10, 177-183;
http://dx.doi.org/10.1002/cbdv.201200406
b) Zou M., Yu S.-S., Wang K., Zhang D.-Y., Wu X.-M., Hua W.-Yi. Chin. J. Nat. Med. 2013, 11, 289-295;
c) Hutt O.E., Doan T.L., Georg G.I. Organic Lett. 2013, 15, 1602-1605;
http://dx.doi.org/10.1021/ol400385w
d) Zhu S.-L., Wu Y., Liu C.-J., Wei C.-Y., Tao J.-C., Liu H.-M. Eur. J. Med. Chem. 2013, 65, 70-82;
http://dx.doi.org/10.1016/j.ejmech.2013.04.044
e) Zhu S.-L., Wu Y., Liu C.-J., Wei C.-Y., Tao J.-C., Liu H.-M. Bioorg. Med. Chem. Lett. 2013, 23, 1343-1346;
http://dx.doi.org/10.1016/j.bmcl.2012.12.091
f) Ma Z.-W., Wu Y., Sun B., Du H.-L., Shi W.-M., Tao J.-C. Tetrahedron: Asymmetry 2013, 24, 7-13;
http://dx.doi.org/10.1016/j.tetasy.2012.11.009
g) Geng Z.-C., Chen X., Zhang J.-X., Li N., Chen J., Huang X.-F., Zhang S.-Y., Tao J.-C., Wang X.-W. Eur. J. Org. Chem. 2013, 22, 4738-4743.
http://dx.doi.org/10.1002/ejoc.201300524

 

4. a) Strobykina I.Yu., Garifullin B.F., Kovylyaeva G.I., Musin R.Z., Gubaidullin A.T., Kataev V.E. Russ. J. Gen. Chem. 2007, 77, 1066-1068;
http://dx.doi.org/10.1134/S1070363207060205
b) Garifullin B.F., Strobykina I.Yu., Lodochnikova O.A., Musin R.Z., Gubaidullin A.T., Kataev V.E. Chem. Natur. Compd. 2011, 47, 422-427;
http://dx.doi.org/10.1007/s10600-011-9949-6
c) Khaybullin R.N., Strobykina I.Yu., Gubskaya V.P., Fazleeva G.М., Latypov Sh.K., Kataev V.E. Mendeleev Commun. 2011, 21, 134-136;
http://dx.doi.org/10.1016/j.mencom.2011.04.006
d) Korochkina M.G., Nikitashina A.D., Khaibullin R.N., Petrov K.A., Strobykina I.Yu., Zobov V.V., Kataev V.E. Med. Chem. Commun. 2012, 3, 1449-1454;
http://dx.doi.org/10.1039/c2md20165h
e) Garifullin B.F., Andreeva O.V., Strobykina I.Yu., Babaev V.M., Kataev V.E. Macroheterocycles 2013, 6, 184-191.
http://dx.doi.org/10.6060/mhc130334k

 

5. a) Breitmaier E. Terpenes. Wiley, 2006, 214 p.
http://dx.doi.org/10.1002/9783527609949
b) Shi Q.-W., Su X.-H., Kiyota H. Chem. Rev. 2008, 108, 4295-4327;
http://dx.doi.org/10.1021/cr078350s
c) Ferreira M.J.U., Duarte N., Lage H., Molnár J. Reversal of Multidrug Resistance by Macrocyclic and Polycyclic Diterpenoids from Euphorbia species, Ch. 8. In: Recent Progress in Medicinal Plants. Vol. 32. Ethnomedicine and Therapeutic Validation. (Kaushik G., Govil J.N., Eds.), Houston: Studium Press Lic., 2012, 448 p.

 

6. a) Bruker. Area detector control and integration software. Version 5.x. In: SMART and SAINT. Madison, Wisconsin (USA): Bruker Analytical X-ray Instruments Inc.; 1996;
b) Bruker. APEX2 Software Suite for Crystallographic Programs, Bruker AXS, Inc., Madison, WI, USA, 2009;
c) Sheldrick G.M., SHELX-97: Programs for Crystal Structure Analysis, University of Göttingen, Institut für Anorganische Chemie der Universität, Tammanstrasse 4, D-3400 Göttingen, Germany, 1997;
d) Sheldrick G.M. Acta Cryst., A 2008, 64. 112-122;
http://dx.doi.org/10.1107/S0108767307043930
e) Farrugia L.J. WinGX and ORTEP for Windows: an update. J. Appl. Cryst. 2012, 45, 849-854;
http://dx.doi.org/10.1107/S0021889812029111
f) Spek A.L. J. Appl. Cryst. 2003, 36, 7-13;
http://dx.doi.org/10.1107/S0021889802022112
g) Macrae C.F., Edgington P.R., McCabe P., Pidcock E., Shields G.P., Taylor R., Towler M., van de Streek J. J. Appl. Cryst. 2006, 39, 453-457.
http://dx.doi.org/10.1107/S002188980600731X

 

7. Khaibullin R.N., Strobykina I.Yu., Kataev V.E., Lodochnikova O.A., Gubaidullin A.T., Musin R.Z. Russ. J. Gen. Chem. 2009, 79, 967-971.
http://dx.doi.org/10.1134/S107036320905017X

 

8. Al'fonsov V.A., Bakaleinik G.A., Gubaidullin A.T., Kataev V.E., Kovylyaeva G.I., Konovalov A.I., Litvinov I.A., Strobykina I.Y., Strobykin S.I., Andreeva O.V., Korochkina M.G. Russ. J. Gen. Chem. 2000, 70, 953-960.

 

9. Kataev V.E., Militsina O.I., Strobykina I.Yu., Kovylyaeva G.I., Musin R.Z., Fedorova O.V., Rusinov G.L., Zueva M.N., Mordovskoi G.G., Tolstikov A.G. Pharm. Chem. J. 2006, 40, 473-475.
http://dx.doi.org/10.1007/s11094-006-0157-9

 

10. Kataev V.E., Militsina O.I., Strobykina I.Yu., Gubaidullin A.T., Zverev V.V., Kataeva O.N., Fedorova O.V., Valova M.S., Rusinov G.L. J. Incl. Phenom. 2008, 60, 51-58.
http://dx.doi.org/10.1007/s10847-007-9351-y

 

11. a) An Y., Zhang Y.-X., Wu Y., Liu Z.-M., Tao C. Pi. J. Tetrahedron: Asymmetry 2010, 21, 688-694;
http://dx.doi.org/10.1016/j.tetasy.2010.04.019
b) Pariwat P., Homvisasevongsa S., Muanprasat C., Chatsudthipong V. J. Pharm. Exp. Ther. 2008, 324, 798-805;
http://dx.doi.org/10.1124/jpet.107.129288
c) Chen J., Sun M., Cai J., Cao M., Zhou W., Ji M. J. Chem. Crystallogr. 2011, 41, 519-522.
http://dx.doi.org/10.1007/s10870-010-9912-6

 

12. Wu Y., Yang J.-H., Dai G.-F., Liu C.-J., Tian G.-Q., Ma W.-Y., Tao J.-C. Bioorg. Med. Chem. 2009, 17, 1464-1473.
http://dx.doi.org/10.1016/j.bmc.2009.01.017

 

13. Kataev V.E., Strobykin S.I., Timosheva A.P., Al'fonsov V.A., Korochkina M.G., Strobykina I.Yu. Russ. J. Gen. Chem. 2005, 75, 244-247.
http://dx.doi.org/10.1007/s11176-005-0207-0