福山インドール合成
1. Fukuyama indole synthesisThe Fukuyama indole synthesis is the chemical reaction of alkenylthioanilides to give 2,3-disubstituted indoles. Most commonly tributyltin hydride is utilized as the reducing agent, with azobisisobutyronitrile (AIBN) as a radical initiator. Being one of the simplest methods for synthesizing poly-substituted indoles, this procedure has been utilized in numerous natural product syntheses, including aspidophytine, vinblastine and strychnine
Read “Fukuyama indole synthesis” on English Wikipedia
Read “福山インドール合成” on Japanese Wikipedia
Read “Fukuyama indole synthesis” on DBpedia
Read “Fukuyama indole synthesis” on English Wikipedia
Read “福山インドール合成” on Japanese Wikipedia
Read “Fukuyama indole synthesis” on DBpedia
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