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ENANTIONSELECTIVE PROCESSES TO INSECTICIDAL 3-ARYL-3-TRIFLUOROMETHYL-SUBSTITUTED PYRROLIDINES

机译:对杀虫剂3-芳基-3-三氟甲基取代的吡咯烷的抗eniantionsElective方法

摘要

The present invention relates to processes for the enantio-selective preparation of spyrrolidine derivatives useful in the manufacture of pesticidally active compounds, as well as to intermedates in the processes. The processes include those comprising(a-i) reacting a compound of formula IawhereinP is alkyl, aryl or heteroaryl, each optionally substituted, wherein the heteroaryl is connected at P via a ring carbon atom;R1 is chlorodifluoromethyl or trifluoromethyl;R2 is aryl or heteroaryl, each optionally substituted;with a source of cyanide in the presence a chiral catalyst to give a compound of formula IIawherein P, R1 and R2 are as defined for the compound of formula Ia; and(a-ii) oxidising the compound of formula IIa with a peroxy acid, or peroxide in the presence of an acid to give a compound of formula VIwherein R1 and R2 are as defined for the compound of formula Ia.
机译:本发明涉及用于制备杂种活性化合物的筛选衍生物的对筛选制剂的方法,以及该方法中的中间体。 该方法包括包含(AI)的方法,使式IaHONTINP化合物是烷基,芳基或杂芳基,其中芳基或杂芳基,其中杂芳基经由环碳原子在P处连接; R 1是氯二氟甲基或三氟甲基; R 2是芳基或杂芳基, 每种任选地取代;在存在的氰化物源中,给予手性催化剂,得到式IIaIa,R1和R2如式Ia化合物所定义; (A-II)用过氧酸氧化式IIa化合物,或在酸存在下过氧化物,得到式VIININ r1和R2的化合物,如式IA化合物所定义。

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