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Diels-Alder reactions of dihydropyridinones: synthetic entry to the manzamine A tricyclic core

…, M Nakagawa, T Hosaka, K Tanabe, Z Lai…

文献索引:Torisawa; Nakagawa; Hosaka; Tanabe; Lai; Ogata; Nakata; Oishi; Hino Journal of Organic Chemistry, 1992 ,  vol. 57,  # 21  p. 5741 - 5747

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被引用次数: 47

摘要

For the construction of the tricyclic core of manzamine A (l), the Diels-Alder reactions of some dihydropyridinones were surveyed. The N-protecting group of the dihydropyridinone played an important role in achieving a successful Diels-Alder reaction. In view of its electron-withdrawing character as well as its thermal stability, the ptolueneaulfonyl protecting group wa~ found to be best in our syntheais. An effective method for the ...