化学
差向异构体
二甲基甲酰胺
取代基
皮兰
立体选择性
药物化学
生物催化
产量(工程)
立体化学
反应机理
有机化学
溶剂
催化作用
冶金
材料科学
作者
Robin G. F. Giles,Ivan R. Green,Wendell Peter Swigelaar,C. Peter Taylor
摘要
The generality of the high-yielding, stereoselective cyclization of 2-allyl-3-(1′-hydroxyethyl)-1,4-dimethoxynaphthalene 1 to afford trans-3,4-dihydro-5,10-dimethoxy-1,3-dimethylnaphtho[2,3-c]pyran 2 is investigated by replacing each of the methoxy groups in the substrate by an ethyl substituent and subjecting these to cyclization reaction conditions identical to those originally reported. For shorter reaction times with potassium tert-butoxide in dimethylformamide under nitrogen, the derived 1-ethyl-, 4-ethyl-, and 1,4-diethylnaphthalenes all cyclize to the trans-1,3-dimethyl compounds, whereas longer times yield increasing proportions of the corresponding cis-isomers. Under air, the epimeric C4 alcohols rel-(1R,3R,4S)-3,4-dihydro-5-ethyl-4-hydroxy-10-methoxy-1,3-dimethylnaphtho[2,3-c]pyran 50 and its rel-(1R,3R,4R) isomer 51 are also isolated from 2-allyl-1-ethyl-3-(1′-hydroxyethyl)-4-methoxynaphthalene 11. The half-chair conformation of pyran 50 is inverted relative to that of its C4 epimer 51.
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