Site-selective and regioselective Diels-Alder reaction of allenyl aryl ethers

摘要

The site-selectivity and regioselectivity of Diels-Alder reactions of allenyl aryl ethers with cyclopenta-diene and acrolein were studied. While cyclopentadiene (as an electron-rich diene) only reacted with the external double bond of allenyl aryl ethers to provide the site-selective normal electron demand Diels-Alder cycloadducts, acrolein (as an electron-deficient diene) reacted with the C1-C2 π bond of allenyl aryl ethers to provide the site- and regioselective hetero-Diels-Alder cycloadducts as exclusive products.