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Synfacts 2011(5): 0501-0501
DOI: 10.1055/s-0030-1259799
DOI: 10.1055/s-0030-1259799
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag
Stuttgart ˙ New York
Everything is Falling into Place!
K. Motokuni, T. Okada, D. Takeuchi, K. Osakada*
Tokyo Institute of Technology, Yokohama, Japan
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
15. April 2011 (online)
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Significance
The Brookhart catalyst system is shown to efficiently catalyze the cyclopolymerization of functionalized trienes. The resulting polymers exclusively exhibit racemo (rather than meso) stereochemistry and display modest tacticity. The authors propose that the high stereoselectivity is a result of the rapid rate of migratory insertion versus the rate of β-hydride elimination during the cyclization process. The post-polymerization hydrolysis of a cyclic acetal functional group is also described, thus permitting access to additional modifications.