메뉴 건너뛰기




Volumn 27, Issue 16, 2008, Pages 4260-4264

Novel straightforward access to a 2,2′-bipyridine ligand bearing two "(η2-dppe)(η5-C5Me 5)FeC≡C-" redox-active substituents by homocoupling of mononuclear organoiron(II) 2-bromopyridyl synthons

Author keywords

[No Author keywords available]

Indexed keywords

BIPYRIDINE LIGANDS; SYNTHESIS AND CHARACTERIZATION;

EID: 51049083601     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om800388j     Document Type: Article
Times cited : (10)

References (44)
  • 13
    • 0038452348 scopus 로고    scopus 로고
    • Several ferrocene derivatives have been reported, though; see for instance: (a) Siemeling, U.; Vor der Brüggen, J.; Vorfeld, U.; Neumann, B.; Stammler, A.; Stammler, H.-G.; Brockhinke, A.; Plessow, R.; Zanello, P.; Laschi, F.; de Biani, F. F.; Fontani, M.; Steenken, S.; Stapper, M.; Gurzadayan, G. Chem. Eur. J. 2003, 9, 2819-2833.
    • Several ferrocene derivatives have been reported, though; see for instance: (a) Siemeling, U.; Vor der Brüggen, J.; Vorfeld, U.; Neumann, B.; Stammler, A.; Stammler, H.-G.; Brockhinke, A.; Plessow, R.; Zanello, P.; Laschi, F.; de Biani, F. F.; Fontani, M.; Steenken, S.; Stapper, M.; Gurzadayan, G. Chem. Eur. J. 2003, 9, 2819-2833.
  • 26
    • 0003944494 scopus 로고
    • Taylor, J. K, Ed, Oxford University Press: Oxford, U.K
    • (b) Campbell, I. B. In Organocopper Reagents-A Practical Approach; Taylor, J. K., Ed.; Oxford University Press: Oxford, U.K., 1994; pp 216-235.
    • (1994) Organocopper Reagents-A Practical Approach , pp. 216-235
    • Campbell, I.B.1
  • 32
    • 51049120294 scopus 로고    scopus 로고
    • The overall yield of 3 obtained from 4 and the noncommercial 5,5′-dibromo-2,2′-bipyridine 5 when the synthesis of 4 from 8 is taken into consideration is below 13, vs 46% for the present route when the synthesis of 6b is undertaken from 8 and 9
    • The overall yield of 3 obtained from 4 and the noncommercial 5,5′-dibromo-2,2′-bipyridine 5 when the synthesis of 4 from 8 is taken into consideration is below 13%, vs 46% for the present route when the synthesis of 6b is undertaken from 8 and 9.
  • 33
    • 0036532565 scopus 로고    scopus 로고
    • Note also that the halogenated reactant 7b can be obtained at the multigram scale in much better yields than 5 according to published procedures; see for instance: Bouillon, A.; Lancelot, J.-C.; Collot, V.; Bovy, P. R.; Rault, S. Tetrahedron 2002, 58, 2885-2890.
    • Note also that the halogenated reactant 7b can be obtained at the multigram scale in much better yields than 5 according to published procedures; see for instance: Bouillon, A.; Lancelot, J.-C.; Collot, V.; Bovy, P. R.; Rault, S. Tetrahedron 2002, 58, 2885-2890.
  • 40
    • 0031059866 scopus 로고    scopus 로고
    • Carter, C. W, Sweet, R. M, Eds, Academic Press: London
    • Otwinowski, Z.; Minor, W. In Methods in Enzymology; Carter, C. W., Sweet, R. M., Eds.; Academic Press: London, 1997; Vol. 276, pp 307-326.
    • (1997) Methods in Enzymology , vol.276 , pp. 307-326
    • Otwinowski, Z.1    Minor, W.2
  • 41
    • 51049092739 scopus 로고    scopus 로고
    • Kappa CCD Software; Nonius BV, Delft, The Netherlands, 1999. CrysAlis/RED, Version 1.171.26pre2 beta ed, Oxford Diffraction Ltd, Oxford, U.K
    • Kappa CCD Software; Nonius BV, Delft, The Netherlands, 1999. CrysAlis/RED, Version 1.171.26pre2 beta ed.; Oxford Diffraction Ltd., Oxford, U.K.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.