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Unpublished results. Interestingly, under similar conditions in a mixed solvent of THF-heptane (1/1, v/v) at -78 °C, polyisoprenyllithium was reacted with a,a'dichloro-p-xylene more efficiently to afford a polyispprene with chloromethylphenyl terminus in 91% yield. In this case, the dimer was formed only in 9% yield.
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85034494520
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A polystyrene having two MMP termini and one bromobutyl terminus was also obtained by reacting polystyryllithium with 3 followed by treatment with a 10-fold excess of 1,4dibromobutane in THF at - 78 °C.
-
A polystyrene having two MMP termini and one bromobutyl terminus was also obtained by reacting polystyryllithium with 3 followed by treatment with a 10-fold excess of 1,4dibromobutane in THF at - 78 °C.
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