Diels–Alder cycloadditions of 3,5-dibrom
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Cheon-Gyu Cho; Yong-Woo Kim; Won-Kyum Kim
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Article
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2001
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Elsevier Science
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French
⚖ 56 KB
Dibromo-2-pyrone underwent facile Diels-Alder [4+2] cycloadditions with cycloalkenyl silyl ethers to provide a series of tricyclolactones, with good to excellent chemical yields and stereoselectivity. The resulting cycloadducts could be readily converted into the corresponding bicarbocycles upon sel