コープ転位
1. Cope rearrangementThe Cope rearrangement is an extensively studied organic reaction involving the 3,3 3,3]-sigmatropic rearrangement of 1,5-dienes. It was developed by Arthur C. Cope. For example 3-methyl-1,5-hexadiene heated to 300°C yields 1,5-heptadiene. The Cope rearrangement causes the fluxional states of the molecules in the bullvalene family.
Read “Cope rearrangement” on English Wikipedia
Read “コープ転位” on Japanese Wikipedia
Read “Cope rearrangement” on DBpedia
Read “Cope rearrangement” on English Wikipedia
Read “コープ転位” on Japanese Wikipedia
Read “Cope rearrangement” on DBpedia
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