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König, Burkhard ; Zieg, H. ; Bubenitschek, P. ; Jones, P. G.

Palladium-Catalyzed Coupling of Vinylferrocene with Aromatic Halides - A Highly Efficient Route to (Ferrocenylvinyl)arenes

König, Burkhard, Zieg, H., Bubenitschek, P. and Jones, P. G. (1994) Palladium-Catalyzed Coupling of Vinylferrocene with Aromatic Halides - A Highly Efficient Route to (Ferrocenylvinyl)arenes. Chemische Berichte 127 (9), pp. 1811-1813.

Date of publication of this fulltext: 05 Aug 2009 13:51
Article
DOI to cite this document: 10.5283/epub.6164


Abstract

(Ferrocenylvinyl)arenes 3, 5, and 7 are obtained from vinylferrocene (1) and substituted aromatic and heteroaromatic halides by palladium-catalyzed Heck-type reactions. Up to three ferrocene units are introduced in one step by the multi-fold reaction of 1,2-dibromo- (4) or 1,3,5-tribromobenzene (6) with 1. The first crystal structure of a bis(ferrocenylvinyl)benzene chromophore (5) is reported.



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Details

Item typeArticle
Journal or Publication TitleChemische Berichte
Volume:127
Number of Issue or Book Chapter:9
Page Range:pp. 1811-1813
Date1994
InstitutionsChemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
Identification Number
ValueType
10.1002/cber.19941270935DOI
KeywordsVinylferrocene , Palladium-catalyzed couplin , (Ferrocenylvinyl)arenes
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgYes
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-61644
Item ID6164

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