首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >One-Pot Synthesis of Spirotetrahydrooxino[3,4-c]pyridines and Spirotetrahydrofuro[3,2-b]pyridin-2-ones via Lactonization from Activated Pyridyldihydroozaxoles and Bis(trimethylsilyl)ketene Acetals
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One-Pot Synthesis of Spirotetrahydrooxino[3,4-c]pyridines and Spirotetrahydrofuro[3,2-b]pyridin-2-ones via Lactonization from Activated Pyridyldihydroozaxoles and Bis(trimethylsilyl)ketene Acetals

机译:活化吡啶基二氢唑和双(三甲基甲硅烷基)乙烯酮缩醛的酯化反应一锅法合成螺四氢氧代[3,4-c]吡啶和螺四氢呋喃[3,2-b]吡啶-2-酮

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摘要

5-Methyl-2-(pyridin-3-yl)-4,5-dihydrooxazole and 5-methyl-2-(pyridin-4-yl)-4,5-dihydrooxazole activated by triflic anhydride underwent lactonization with bis(trimethylsilyl)ketene acetals to provide tetrahydrooxino[3,4-c]pyridines and tetrahydrofuro[3,2-b]pyridin-2-ones. Formation of the product was controlled by the position of the pyridyl substituent at C-3 and C-4 of the pyridyldihydrooxazole. On the other hand, 1-(trifluoromethylsulfonamido)propan-2-yl picolinate was obtained under the same conditions from 5-methyl-2-(pyridin-2-yl)-4,5-dihydrooxazole.
机译:由三氟甲磺酸酐活化的5-甲基-2-(吡啶-3-基)-4,5-二氢恶唑和5-甲基-2-(吡啶-4-基)-4,5-二氢恶唑用双(三甲基甲硅烷基)内酯化乙烯酮缩醛提供四氢氧代[3,4-c]吡啶和四氢呋喃[3,2-b]吡啶-2-酮。通过吡啶基二氢恶唑的C-3和C-4处的吡啶基取代基的位置控制产物的形成。另一方面,在相同条件下从5-甲基-2-(吡啶-2-基)-4,5-二氢恶唑制得1-(三氟甲基磺酰胺基)丙-2-基吡啶甲酸酯。

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