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- W2016367706 abstract "A calix[4]arene derived bis(spirodienone) acts as the 2π component in a cycloaddition reaction with two molecules of 3,5-di-tert-butyl-1,2-benzoquinone in the [2+4] manner leading to macrocycles with a benzodioxin moiety. A theoretical rationalization of the results suggested a sterically encumbered regioselective pathway, which gives sterically crowded products." @default.
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- W2016367706 title "Sterically encumbered regioselective cycloaddition of a calixarene derived bis(spirodienone) with 1,2-benzoquinones" @default.
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- W2016367706 doi "https://doi.org/10.1016/j.tetlet.2005.11.151" @default.
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