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- W2953334100 abstract "Abstract The first intramolecular benzyne Diets-Alder reaction with an acyclic diene is reported. The course of the reaction is dependent on the diene geometry. Trans dienes afford [4+2] cycloadducts; cis dienes apparently give [2+2 ] cycloadducts followed by further rearrangement, a mechanistic course which is supported by deuterium labeling experiments." @default.
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- W2953334100 date "2010-08-12" @default.
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- W2953334100 title "ChemInform Abstract: First Intramolecular Benzyne Diels-Alder Reaction with an Acyclic Diene. Unusual Effect of Diene Geometry on the Course of the Reaction." @default.
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- W2953334100 doi "https://doi.org/10.1002/chin.199614112" @default.
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