化学
催化作用
区域选择性
分子内力
戒指(化学)
迈克尔反应
铂金
药物化学
接受者
高分子化学
有机化学
凝聚态物理
物理
标识
DOI:10.1016/0021-9517(68)90158-9
摘要
We report a novel intramolecular 1,6 oxa-Michael addition on substituted dihydropyridines to obtain 5 and 6 member ring lactones in an one-pot reaction starting from activated pyridinyl propenones, without organic catalysis or presence of bulky groups in the Michael acceptor. A marked dependence on the regioselectivity of ring closure was found, dependent on the propenone used.
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