Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
Author(s)
Detail(s)
Original language | English |
---|---|
Pages (from-to) | 367-369 |
Journal / Publication | Bulletin of the Chemical Society of Japan |
Volume | 78 |
Issue number | 2 |
Publication status | Published - 15 Feb 2005 |
Externally published | Yes |
Link(s)
Abstract
An efficient palladium catalyzed cross coupling of tributyl(vinyl)stannane with dialkoxy and dialkyl substituted 1,4-dihalobenzenes is described. This single-step coupling provides an efficient synthesis of functionalized 2,5-divinylbenzenes, which are useful precursors of 1,4-phenylenevinylene copolymers.
Citation Format(s)
Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction. / Daoud, Walid A.; Turner, Michael L.
In: Bulletin of the Chemical Society of Japan, Vol. 78, No. 2, 15.02.2005, p. 367-369.
In: Bulletin of the Chemical Society of Japan, Vol. 78, No. 2, 15.02.2005, p. 367-369.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review