Palladium‐Catalyzed Coupling of Vinylferrocene with Aromatic Halides — A Highly Efficient Route to (Ferrocenylvinyl)arenes | Zendy

König Burkhard | Zendy; Zieg Harald | Zendy; Bubenitschek Peter | Zendy; Jones Peter G. | Zendy

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

Author(s) -

König Burkhard,

Zieg Harald,

Bubenitschek Peter,

Jones Peter G.

Publication year - 1994

Publication title -

chemische berichte

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.667

H-Index - 136

eISSN - 1099-0682

pISSN - 0009-2940

DOI - 10.1002/cber.19941270935

Subject(s) - chemistry , palladium , halide , ferrocene , benzene , chromophore , catalysis , crystal structure , coupling reaction , heck reaction , organic chemistry , photochemistry , medicinal chemistry , combinatorial chemistry , polymer chemistry , electrode , electrochemistry

(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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