Copper(I)-mediated synthesis of ferrocenyl alkyl ethers

Organometallics

Volumn 29, Issue 18, 2010, Pages 4196-4198

  Schaarschmidt, Dieter ^a   Lang, Heinrich ^a  

^a CHEMNITZ UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYL ETHERS; FERROCENES; FERROCENYL; GOOD YIELD;

ALKYLATION; ETHERS; OXYGEN;

ORGANIC COMPOUNDS;

EID: 77956901477     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om1006209     Document Type: Article

References (25)

1. Ferrocenes: Ligands, Materials and Biomolecules; Stepnicka, P., Ed.; John Wiley & Sons Ltd: Chichester, 2008.
2. Ferrocenes: Homogeneous Catalysis, Organic Synthesis, Material Science; Togni, A., Hayashi, T., Eds.; VCH Verlagsgesellschaft: Weinheim, 1995.
3. Dai, L.-X.; Tu, T.; You, S.-L.; Deng, W.-P.; Hou, X.-L. Acc. Chem. Res. 2003, 36, 659
4. Ferrocene is added to diesel fuel in order to improve combustion and to reduce the emission of soot.
5. Nesmeyanov et al. report that hydroxyferrocene decomposes within several days when exposed to air.
6. Schaarschmidt, D.; Lang, H. Unpublished results.
7. Nesmeyanov, A. N.; Sazanova, V. A.; Drozd, V. N. Tetrahedron Lett. 1959, 17, 13
8. Nesmejanow, A. N.; Ssasonowa, W. A.; Drosd, V. N. Chem. Ber. 1960, 93, 2717
9. Akabori, S.; Sato, M.; Ebine, S. Synthesis 1981, 278
10. Akabori, S.; Ohtomi, M.; Sato, M.; Ebine, S. Bull. Chem. Soc. Jpn. 1983, 56, 1455
11. Singewald, E. T.; Mirkin, C. A.; Stern, C. L. Angew. Chem., Int. Ed. Engl. 1995, 34, 1624
12. Anderson, J. C.; Blake, A. J.; Arnall-Culliford, J. C. Org. Biomol. Chem. 2003, 1, 3586
13. an der Heiden, M. R.; Frey, G. D.; Plenio, H. Organometallics 2004, 23, 3548
14. Schaarschmidt, D.; Lang, H. Eur. J. Inorg. Chem. 2010, accepted, doi: 10.1002/ejic.201000722.
15. Schaarschmidt, D.; Lang, H. DE Patent 10 2010 001 364.1, 2010.
16. Shafir, A.; Lichtor, P. A.; Buchwald, S. L. J. Am. Chem. Soc. 2007, 129, 3490
17. Özciubukcisu, S.; Schmitt, E.; Leifert, A.; Bolm, C. Synthesis 2007, 389
18. Changing the solvent to acetonitrile or dmso did not affect the yield positively.
19. Naidu, A. B.; Sekar, G. Tetrahedron Lett. 2008, 49, 3147
20. Niu, J.; Zhou, H.; Li, Z.; Xu, J.; Hu, S. J. Org. Chem. 2008, 73, 7814
21. Wolter, M.; Nordmann, G.; Job, G. E.; Buchwald, S. L. Org. Lett. 2002, 4, 973
22. Naidu, A. B.; Jaseer, E. A.; Sekar, G. J. Org. Chem. 2009, 74, 3675
23. Chang, J. W. W.; Chee, S.; Mak, S.; Buranaprasertsuk, P.; Chavasiri, W.; Chan, P. W. H. Tetrahedron Lett. 2008, 49, 2018
24. Zhang, H.; Ma, D.; Cao, W. Synlett 2007, 243
25. Tye, J. W.; Weng, Z.; Giri, R.; Hartwig, J. F. Angew. Chem. 2010, 122, 2231