Matches in DBpedia 2016-04 for { ?s ?p "The Cope rearrangement is an extensively studied organic reaction involving the [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."@en }
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- Cope_rearrangement abstract "The Cope rearrangement is an extensively studied organic reaction involving the [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.".
- Q905087 abstract "The Cope rearrangement is an extensively studied organic reaction involving the [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.".
- Cope_rearrangement comment "The Cope rearrangement is an extensively studied organic reaction involving the [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.".
- Q905087 comment "The Cope rearrangement is an extensively studied organic reaction involving the [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.".