The diels-alder reaction of a 2,2-dimethoxyethyl ester via a cationic intermediate
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Add time:09/07/2019 Source:sciencedirect.com
2,2-Dimethoxyethyl acrylate, which is easily prepared by the Mitsunobu reaction, reacts with dienes at −78 °C in the presence of a Lewis acid such as titanium(IV) chloride to afford the corresponding DielsAlder adducts in high yields.
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