辻・トロスト反応
1. Tsuji–Trost reactionThe Tsuji–Trost reaction is a palladium-catalysed substitution reaction of a nucleophile with a substrate containing a leaving group in an allylic position. The nucleophile can be carbon, nitrogen or oxygen based. Examples are alcohols, enolates, phenols and enamines. The leaving group can for example be a halide or acetate. A base is required for in-situ generation of the nucleophile from a precursor. In the reaction product the nucleophile has replaced the leaving group.
Read “Tsuji–Trost reaction” on English Wikipedia
Read “辻・トロスト反応” on Japanese Wikipedia
Read “Tsuji–Trost reaction” on DBpedia
Read “Tsuji–Trost reaction” on English Wikipedia
Read “辻・トロスト反応” on Japanese Wikipedia
Read “Tsuji–Trost reaction” on DBpedia
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