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• W2949654368 abstract "A study on the synthetic utility of [6+3] cycloaddition of pentafulvenes with 3-oxidopyrylium betaines is described. 5–8 Fused oxa-bridged cyclooctanoids, the products of the above methodology undergo facile Diels–Alder reaction, dipolar cycloaddition, Luche reduction and selective hydrogenation over Pd/C leading to functionalized molecules, which can be transformed to oxa-bridged fused cyclooctanoids. We have shown that the carbon framework of the molecules can be directly expanded from the product, thus enhancing the synthetic versatility of the products." @default.
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• W2949654368 date "2006-12-01" @default.
• W2949654368 modified "2023-09-23" @default.
• W2949654368 title "Studies on the synthetic utility of [6+3] cycloaddition of pentafulvenes with 3-oxidopyrylium betaines: efficient synthesis of fused ring cyclooctanoids" @default.
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• W2949654368 doi "https://doi.org/10.1016/j.tet.2006.09.102" @default.
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