Asymmetrical induction in the synthesis of ferrocenyl-substituted bicyclicpyrazolines. E,Z-isomerization of the ferrocenylmethylidene fragment

Citation
Ei. Klimova et al., Asymmetrical induction in the synthesis of ferrocenyl-substituted bicyclicpyrazolines. E,Z-isomerization of the ferrocenylmethylidene fragment, RUSS CHEM B, 48(4), 1999, pp. 761-766
Citations number
13
Categorie Soggetti
Chemistry
Journal title
RUSSIAN CHEMICAL BULLETIN
ISSN journal
10665285 → ACNP
Volume
48
Issue
4
Year of publication
1999
Pages
761 - 766
Database
ISI
SICI code
1066-5285(199904)48:4<761:AIITSO>2.0.ZU;2-6
Abstract
Asymmetrical induction in the synthesis of bicyclic ferrocenyl-substituted pyrazolines was studied. High diastereoselectivity of induction of the chir al center by the chiral center of the 1,2 type was observed. The cis diaste reomer of 2-acetyt-3-ferrocenyl-7-ferrocenylmethylidene-2,3,3a,4,5,6,7-hept ahydroindazole was studied by X-ray diffraction analysis. The E,Z-configura tional isomerism of the ferrocenylmethylene fragment of pyrazolines in an a cidic medium is described.