福山カップリング
1. Fukuyama couplingThe Fukuyama coupling is a coupling reaction taking place between a thioester and an organozinc halide in the presence of a palladium catalyst. The reaction product is a ketone. This reaction was discovered by Tohru Fukuyama et al. in 1998 . Advantages are high chemoselectivity, mild reaction conditions and the use of less-toxic reagents . One advantage of this method is that the reaction stops at the ketone and does not proceed to a tertiary alcohol.
Read “Fukuyama coupling” on English Wikipedia
Read “福山カップリング” on Japanese Wikipedia
Read “Fukuyama coupling” on DBpedia
Read “Fukuyama coupling” on English Wikipedia
Read “福山カップリング” on Japanese Wikipedia
Read “Fukuyama coupling” on DBpedia
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