Formation of functionalized [3]ferrocenophane derivatives by an enamine condensation reaction-Reference-Cited by-同舟云学术

Formation of functionalized [3]ferrocenophane derivatives by an enamine condensation reaction

Published:1999-09 Issue:2 Volume:586 Page:218-222
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Knüppel Stephanie,Fröhlich Roland,Erker Gerhard

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference10 articles.

1. (a) A. Eisenstadt, M. Cais, Isr. J. Chem. 5 (1967) 37p. (b) T.D. Turbitt, W.E. Watts, J. Organomet. Chem. 46 (1972) 109. (c) P. Dodey, B. Gautheron, C.R. Hebd. Seance Acad. Sci. Ser. C (1975) 1113. (d) W. Crawford, T.D. Turbitt, W.E. Watts, J. Organomet. Chem. 105 (1976) 341.

2. (a) M. Sališová, Š. Toma, E. Sołčániová, J. Organomet. Chem. 132 (1977) 419. (b) E. Gyepes, T. Glowiak, Š. Toma, J. Soldánová, J. Organomet. Chem. 276 (1984) 209. (c) E. Gyepes, T. Glowiak, Š. Toma, J. Organomet. Chem. 316 (1986) 163.

3. For two formally related aldol examples see: (a) M. Sališova, Š. Toma, E. Sołčániová, Coll. Czech. Chem. Commun. 45 (1980) 1290. (b) Y. Omote, R. Kobayashi, Y. Nakada, N. Sugiyama, Bull. Chem. Soc. Jpn. 46 (1973) 3315. For indications of a reversible intramolecular aldol coupling of 10 see: (c) C.R. Hauser, C.E. Cain, J. Org. Chem. 23 (1958) 1142. (d) C.E. Cain, T.A. Mashburn, C.R. Hauser, J. Org. Chem. 26 (1961) 1030. (e) C.R. Hauser, T.A. Mashburn, J. Org. Chem. 26 (1961) 1795.

4. (a) I.M. Paushkin, L.S. Polak, T.P. Vishnyakova, I.I. Patalakh, F.F. Macchus, T.A. Sokolinskaya, J. Polym. Sci. C 4 (1963) 1481. (b) H. Kono, M. Shiga, I. Motoyama, K. Hata, Bull. Chem. Soc. Jpn. 42 (1969) 3267. (c) A. Kasahara, T. Izumi, I. Shimizu, Chem. Lett. (1979) 1317. (d) S. Kamiyama, A. Kasahara, T. Izumi, I. Shimizu, H. Watabe, Bull. Chem. Soc. Jpn. 54 (1981) 2079. (e) J. Mirek, S. Rachwał, T. Górecki, B. Kawałek, P. Milart, E. Szneler, J. Organomet. Chem. 344 (1988) 363. (f) J.J.C. Erasmus, G.J. Lamprecht, J.C. Swarts, A. Roodt, A. Oskarsson, Acta Crystallogr. C 52 (1996) 3000.

5. In contrast, Michael additions are frequently used to prepare [5]ferrocenophanes or larger ring systems. For examples see: (a) T.A. Mashburn, C.E. Cain, C.R. Hauser, J. Org. Chem. 25 (1960) 1982. (b) M. Furdik, Š. Toma, J. Suchy, P. Elecko, Chem. Zvesti, 15 (1961) 45. (c) Š. Toma, A. Gaplovsky, Coll. Czech. Chem. Commun. 47 (1983) 1988. (d) R. Dabard, H. Patin, Bull. Soc. Chim. Fr. (1973) 2158. (e) I.H. Barr, W.E. Watts, Tetrahedron 24 (1968) 3219.

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