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Ferrocene Compounds. I. Acetylferrocene and Diethyl Oxalate Condensation Products and Their Derivatives

M. Laćan ; Laboratory of Organic Chemistry and Technology, Biochemistry Department, Faculty of Technology, University of Zagreb
V. Rapić ; Laboratory of Organic Synthesis, Institute of Food Science and Technology, Zagreb, Croatia, Yugoslavia

Puni tekst: engleski, pdf (6 MB) str. 411-416 preuzimanja: 488* citiraj
APA 6th Edition
Laćan, M. i Rapić, V. (1970). Ferrocene Compounds. I. Acetylferrocene and Diethyl Oxalate Condensation Products and Their Derivatives. Croatica Chemica Acta, 42 (3), 411-416. Preuzeto s https://hrcak.srce.hr/197530
MLA 8th Edition
Laćan, M. i V. Rapić. "Ferrocene Compounds. I. Acetylferrocene and Diethyl Oxalate Condensation Products and Their Derivatives." Croatica Chemica Acta, vol. 42, br. 3, 1970, str. 411-416. https://hrcak.srce.hr/197530. Citirano 07.04.2020.
Chicago 17th Edition
Laćan, M. i V. Rapić. "Ferrocene Compounds. I. Acetylferrocene and Diethyl Oxalate Condensation Products and Their Derivatives." Croatica Chemica Acta 42, br. 3 (1970): 411-416. https://hrcak.srce.hr/197530
Harvard
Laćan, M., i Rapić, V. (1970). 'Ferrocene Compounds. I. Acetylferrocene and Diethyl Oxalate Condensation Products and Their Derivatives', Croatica Chemica Acta, 42(3), str. 411-416. Preuzeto s: https://hrcak.srce.hr/197530 (Datum pristupa: 07.04.2020.)
Vancouver
Laćan M, Rapić V. Ferrocene Compounds. I. Acetylferrocene and Diethyl Oxalate Condensation Products and Their Derivatives. Croatica Chemica Acta [Internet]. 1970 [pristupljeno 07.04.2020.];42(3):411-416. Dostupno na: https://hrcak.srce.hr/197530
IEEE
M. Laćan i V. Rapić, "Ferrocene Compounds. I. Acetylferrocene and Diethyl Oxalate Condensation Products and Their Derivatives", Croatica Chemica Acta, vol.42, br. 3, str. 411-416, 1970. [Online]. Dostupno na: https://hrcak.srce.hr/197530. [Citirano: 07.04.2020.]

Sažetak
By the reaction of acetylferrocene with diethyl oxalate l ,6-
diferrocenyl-1,3,4,6-hexanetetrone (I), a, y-dioxo-y-ferrocenylbutyric
acid (II) and its ethyl ester (III) were prepared in a yield of 78.3,
55.1 and 51.5°/o resp. The polyoxo compounds I, II and III were
converted through the action of suitable reagents into 2,3-bis
(ferrocenoy lmethy l)quinoxaline (IV), 5,5' (3')-diferroceny 1-1, 1' -dipheny
l-3,3' (5')-dipyrazoly l (V), 3(5)-ferrocenyl-1-phenyl-5(3)-pyrazolecarboxylic acid (VI) and its ethyl ester (VII) and 3-ferrocenoylmethylene- 2-piperazinone (VIII).

Hrčak ID: 197530

URI
https://hrcak.srce.hr/197530

Posjeta: 518 *