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- W1991426414 abstract "The [4+2]-cycloaddition reaction of 3-olefinic oxindoles with a tetraenamine intermediate is presented. In the reaction, a novel class of highly functionalized spirocyclic cyclohexanes with four stereocenters is formed in high yield and excellent stereoselectivity. Mechanistic investigations and calculations point to a stepwise mechanism involving tetraenamine intermediates. Furthermore, several transformations are presented." @default.
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- W1991426414 date "2014-01-01" @default.
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- W1991426414 title "Organocatalytic [4+2] addition reactions via tetraenamine intermediate" @default.
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- W1991426414 doi "https://doi.org/10.1039/c4sc00081a" @default.
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