Research Article. Precursor Synthesis of Some New Macrocyclic Compounds

1. Ogoshi T - Pillarenes, in Gale P, Steed J (eds): Monographs in Supramolecular Chemistry no. 18, Royal Society of Chemistry, Cambridge, UK, 2016, 1-3;Search in Google Scholar

2. Madhavan N,Takatani T, Sherrill CD, Weck M - Macrocyclic cyclooctenesupported AlCl-salen catalysts for conjugated addition reactions: effect of linker and support structure on catalysis. Chem Eur J. 2009;15:1186-1194;10.1002/chem.20080161119101958Search in Google Scholar

3. Grossmann A, Bartlett S, Janecek M, Hodgkinson JT, Spring DR - Diversity-oriented synthesis of drug-like macrocyclic scaffolds using an orthogonal organo- and metal catalysis strategy. Angew Chem Int Ed. 2014;53:13093-13097;10.1002/anie.20140686525257387Search in Google Scholar

4. Li ZP, Liu BH - The use of macrocyclic compounds as eletrocatalysts in fuel cells. J Appl Electrochem. 2010;40:475-483;10.1007/s10800-009-0028-7Search in Google Scholar

5. Prasanna deSilva A - Molecular logic-based computation, in Gale P, Steed J (eds): Monographs in Supramolecular Chemistry no. 12, Royal Society of Chemistry, Cambridge, UK, 2012, 35-36;Search in Google Scholar

6. Ballardini R, Balzani V, Credi A, Gandolfi MT; Kotzyba-Hilbert F, Lehn J-M, Prodi L - Supramolecular Photochemistry and Photophysics. A Cylindrical Macrotricyclic Receptor and its Adducts with Protons, Ammonium Ions, and a Pt(II) Complex. J Am Chem Soc. 1994;116:5741-5746;10.1021/ja00092a026Search in Google Scholar

7. Jyothi RK, Lee JY - The role of macrocyclic compounds in the extraction and possible separation of platinum and rhodium from chloride solutions. Sci Rep. 2016;6;27668:1-14;10.1038/srep27668490134127283394Search in Google Scholar

8. You L, An R, Liang K, Cui B, Wang X - Macrocyclic Compounds: Emerging Opportunities for Current Drug Discovery. Curr Pharm Des. 2016;22:4086-4093;10.2174/138161282266616020411483826845327Search in Google Scholar

9. Mallinson J, Collins I - Macrocycles in new drug discovery. Future Med Chem. 2012;4:1409-1438;10.4155/fmc.12.9322857532Search in Google Scholar

10. Ning CQ, Lu C, Yu NF et al. - Macrocyclic compounds as anti-cancer agents: Design and synthesis of multi-acting inhibitors against HDAC, FLT3 and JAK2. Eur J Med Chem. 2015;95:104-115;10.1016/j.ejmech.2015.03.03425800646Search in Google Scholar

11. Wanninger S, Lorenz V, Subhan A, Edelmann FT - Metal complexes of curcumin -synthetic strategies, structures and medicinal applications. Chem Soc Rev. 2015;44:4986-5002;10.1039/C5CS00088B25964104Search in Google Scholar

12. Balog M, Grosu I, Ple G, Ramondenc Y, Condamine E, Varga RA - Design and Synthesis of New Macrocyclic Cyclophanes Using 1,3-Dioxane Units as Bridges: A Molecular “Rocking Chair”. J Org Chem. 2004;69:1337-1345;10.1021/jo035398714961688Search in Google Scholar

13. Bogdan N, Grosu I, Benoit G, Toupet L, Ramondenc Y, Condamine E, Silaghi-Dumitrescu I, Ple G - Molecular Rotors: Design, Synthesis, Structural Analysis, and Silver Complex of New [7.7]Cyclophanes. Org Lett. 2006;8:2619-2622;10.1021/ol061084516737328Search in Google Scholar

14. Collin JP, Dietrich-Buchecker C, Gavina P, Jimenez-Molero MC, Sauvage JP - Shuttles and Muscles: Linear Molecular Machines Based on Transition Metals. Acc Chem Res. 2001;34:477-487;10.1021/ar000176611412084Search in Google Scholar

15. Badjic JD, Balzani V, Credi A, Silvi S, Stoddart JF - A Molecular Elevator. Science. 2004;303:1845-1849;10.1126/science.109479115031499Search in Google Scholar

16. Leigh DA, Wong JKY, Dehez F, Zerbetto F - Unidirectional rotation in a mechanically interlocked molecular rotor. Nature. 2003;424:174-179;10.1038/nature0175812853952Search in Google Scholar

17. Kocsis I, Hădade N, Grosu I - Synthesis and structural analysis of some new arylbromide decorated azobenzene derivatives. Studia UBB Chemia. 2012;LVII(4):101-107;Search in Google Scholar

18. Liu F, Morokuma K - Computational study on the working mechanism of a stilbene light-driven molecular rotary motor: sloped minimal energy path and unidirectional nonadiabatic photoisomerization. J Am Chem Soc. 2012;134:4864-4876;10.1021/ja211441n22329590Search in Google Scholar

19. Merino E, Ribagorda M - Control over molecular motion using cistrans photoisomerization of the azo-group. Beilstein J Org Chem. 2012;8:1071-1090;10.3762/bjoc.8.119345872423019434Search in Google Scholar

20. Xia SH, Cui G, Fang WH, Thiel W - How photoisomerization drives peptide folding and unfolding: Insights from QM/MM and MM dynamics simulations. Angew Chem Int Ed. 2016;55:2067-2072;10.1002/anie.20150962226836339Search in Google Scholar

21. Kazemi F, Massah AR, Javaherian M - Chemoselective and scalable preparation of alkyl tosylates under solvent-free conditions. Tetrahedron. 2007;63:5083-5087;10.1016/j.tet.2007.03.083Search in Google Scholar

22. Grosu I, Bogdan E, Plé G, Toupet L, Ramondenc Y, Condamine E, Peulon-Agasse V, Balog M - Synthesis and structure of a new macrocycles including spiro-1,3-dioxane units. Eur J Org Chem. 2003;2003(16):3153-3161;10.1002/ejoc.200200615Search in Google Scholar

23. Wang CD, Shi XZ, Xie RJ - Synthesis of diacetals of 2,2-bis(hydroxymethyl)-1,3-propanediol under microwave irradiation. Synth Commun. 17;27(14):2517-2520;10.1080/00397919708004115Search in Google Scholar

24. Grosu I, Mager S, Plé G, Horn P - Axial and helical chirality of some spiro-1,3-dioxanes. J Chem Soc, Chem Commun. 1995;1995:167-168;10.1039/C39950000167Search in Google Scholar

25. Gâz ŞA, Condamine E, Bogdan N, Terec A, Bogdan E, Ramondenc Y, Grosu I - Synthesis and stereochemistry of some new spiro and polyspiro-1,3-dithiane derivatives. Tetraheron. 2008;64: 7295-7300;10.1016/j.tet.2008.05.065Search in Google Scholar