縮甲醛化的 的英文怎麼說
中文拼音 [suōjiǎquánhuàde]
縮甲醛化的
英文
formalized-
Studies on the structure optimization of bis - schiff base deri ved from 4 - amino - antipyrine and 1, 4 - benzenedialdehyde and spectra properties of the ligand with co
氨基安替比林縮對苯二甲醛雙希夫堿的結構優化及其與鈷離子作用的光譜研究An one - pot process including direct condensation of ethyl isodehydracetate and hydrocitronellal, followed by decarboxylation, isomerization and isomer resolution, was developed for practical preparation of zr juvenile hormone analogue series with high content of effective component
以異脫氫乙酸乙酯與甲氧基香茅醛直接縮合為起點,將縮合、脫羧、異構化、 (順、反)異構體拆分等採用多步反應連續一鍋法的操作方法,成功地得到高有效含量的zr型保幼激素類似物。The barnidipine hydrochloride were prepared via cyclocondensation from m - nitrobenzaldehyde, methyl acetoacetate and anmmonium bicarbonate, hydrolysis, esterification with opticaliy ( s ) - n - benzyl - 3 - py - rrolidinol, recrystallisation and salification
摘要研究了以碳酸氫銨,間硝基苯甲醛和乙酰乙酸甲酯為原料,經縮合、部分水解,再與( s ) - n -芐基3 -羥基吡咯烷經酯化、分步重結晶、成鹽得到鹽酸巴尼地平的工藝路線。Cratoneuron taihangense musci : amblystegiaceae, a new species from hebei province, china
二甲基甲酰胺二異丙基縮醛對羧酸酯化反應的研究A facile method for the preparation of 10 - arylmethylene anthrone is reported. when anthrone react with aryl aldehyde in the presence of pyridine by using xylene as the solvent, besides 10 - arylmethylene anthrone derivatives we found other oxygenated anthrone which have not been reported. physical methods shows that the oxygenated anthrone is anthraquinone, and the anthraquinone cannot be removed from the condensed products by recrystallization with solvents. an effective method of getting ride of anthraquinone is sublimation by heating
以蒽酮和芳香醛為原料,二甲苯為溶劑,吡啶催化法制取10 -芳香基甲叉基蒽酮.發現其生成物中除含有目標化合物10 -芳香基甲叉基蒽酮外,還含有部分文獻中沒有報道的蒽酮氧化物,經物理方法確定其為蒽醌.該化合物不能用溶劑重結晶的方法將其從縮合產物中除去,有效的分離方法是升華The promotion action of ionic liquid as an accelerant in synthesizing benzaldehyde ethanediol acetal and benzaldehyde propanediol acetal was studied
摘要以離子液體為促進劑,強酸性聚苯乙烯732催化了苯甲醛與兩種二元醉的縮醛反應。Fluoroalkyl acetic acids were converted to their corresponding carbonyl chlorides, which was then reacted with o - amino benzaldehyde and ammonia gas to give 3 - ( 1 - iminofluoroalkyl ) - 1h - qunolin - 2 - ones in moderate yields
摘要用2 -氟烷基乙酸為初始原料,用氯化亞碸或五氯化磷將其轉化為相應的酰氯,後者在室溫與鄰胺基苯甲醛縮合,通入氨氣迴流反應得到3 - ( 1 -亞胺基氟烷基) 1h -喹啉2 -酮類化合物,產率中等。分享友人