Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
具有环丙基结构的三唑醇类化合物的抗真菌活性。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
具有环丙基结构的三唑醇类化合物的抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑类、三唑类、烯丙胺类、抗生素类等全身用抗真菌药的发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属三唑类杀菌剂,可抑制真菌中麦角甾醇的生物合成,主要商品有:立克莠、富力库、菌立克三种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳基-5-巯基-1,3,4-三唑为原料,在稀碱存在下与二卤代烷反应合成10个新的标题化合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
1,2,4三唑酮3(TO)衍生物的合成,结果表明TO在多种硝化条件下均可制得3硝基1,2,4三唑酮5(NTO),同时还合成
TO的二取代硝基苯衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
研究具有环丙的三唑醇类化合物的抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑类、三唑类、烯丙胺类、抗生素类等全身用抗真菌药的研发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属三唑类杀菌剂,可抑制真菌中麦角甾醇的生物合成,主要商品有:立克莠、富力库、菌立克三种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳-5-巯
-1,3,4-三唑为原料,
存
下与二卤代烷反应合成了10个新的标题化合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
研究了1,2,4三唑酮3(TO)衍生物的合成,果表明TO
多种硝化条件下均可制得3硝
1,2,4三唑酮5(NTO),同时还合成了TO的二取代硝
苯衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
具有环丙基结构的三唑醇类化合物的抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑类、三唑类、烯丙胺类、抗生素类等全身用抗真菌药的发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属三唑类杀菌剂,可抑制真菌中麦角甾醇的生物合成,主要商品有:立克莠、富力
、菌立克三种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳基-5-巯基-1,3,4-三唑为原料,在稀碱存在下与烷反应合成了10个新的标题化合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
了1,2,4三唑酮3(TO)衍生物的合成,结果表明TO在多种硝化条件下均可制得3硝基1,2,4三唑酮5(NTO),同时还合成了TO的
取
硝基苯衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不表本软件的观点;若发现问题,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
研究具有环丙的三唑醇类化合物的抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑类、三唑类、烯丙胺类、抗生素类等全身用抗真菌药的研发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属三唑类杀菌剂,可抑制真菌中麦角甾醇的生物合成,主要商品有:立克莠、富力库、菌立克三种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳-5-巯
-1,3,4-三唑为原料,
存
下与二卤代烷反应合成了10个新的标题化合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
研究了1,2,4三唑酮3(TO)衍生物的合成,果表明TO
多种硝化条件下均可制得3硝
1,2,4三唑酮5(NTO),同时还合成了TO的二取代硝
苯衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
研究具有环丙基结构的唑醇类
合物的抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑类、唑类、烯丙胺类、抗生素类等全身用抗真菌药的研发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属
唑类杀菌剂,可抑制真菌中麦角甾醇的生物合成,主要商品有:立克莠、富力库、菌立克
种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳基-5-巯基-1,3,4-唑为原料,在稀碱存在下与二卤代烷反应合成
10
的标题
合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
研究1,2,4
唑酮3(TO)衍生物的合成,结果表明TO在多种硝
条件下均可制得3硝基1,2,4
唑酮5(NTO),同时还合成
TO的二取代硝基
衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
研究具有环丙基结构醇类化合物
抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪类、
类、烯丙胺类、抗生素类等全身用抗真菌药
研发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
醇属
类杀菌剂,可抑制真菌中麦角甾醇
生物合成,主要商品有:立克莠、富力库、菌立克
种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳基-5-巯基-1,3,4-,在稀碱存在下与二卤代烷反应合成了10个新
标题化合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
研究了1,2,4酮3(TO)衍生物
合成,结果表明TO在多种硝化条件下均可制得3硝基1,2,4
酮5(NTO),同时还合成了TO
二取代硝基苯衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件观点;若发现问题,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
具有环丙基结构的三唑醇类化合物的抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑类、三唑类、烯丙胺类、抗生素类等全身用抗真菌药的发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属三唑类杀菌剂,可抑制真菌中麦角甾醇的生物合成,主要商品有:立克莠、富力
、菌立克三种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳基-5-巯基-1,3,4-三唑为原料,在稀碱存在下与烷反应合成了10个新的标题化合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
了1,2,4三唑酮3(TO)衍生物的合成,结果表明TO在多种硝化条件下均可制得3硝基1,2,4三唑酮5(NTO),同时还合成了TO的
取
硝基苯衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不表本软件的观点;若发现问题,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
研究具有环丙基结构的唑醇类
合物的抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑类、唑类、烯丙胺类、抗生素类等全身用抗真菌药的研发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属
唑类杀菌剂,可抑制真菌中麦角甾醇的生物合成,主要商品有:立克莠、富力库、菌立克
种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳基-5-巯基-1,3,4-唑为原料,在稀碱存在下与二卤代烷反应合成了10个新的
合物。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
研究了1,2,4唑酮3(TO)衍生物的合成,结果表明TO在多种硝
条件下均可制得3硝基1,2,4
唑酮5(NTO),同时还合成了TO的二取代硝基苯衍生物。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问,欢迎向我们指正。
Objective:To study the antifungal activity of triazole alcohols by introduction of cyclopropyl as side chain.
研究具有环丙基结构三唑醇
化合
抗真菌活性。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
介绍咪唑、三唑
、烯丙胺
、抗
全身用抗真菌药
研发进展及市场应用趋势。
Tebuconazole, which belongs to triazole fungicide, can inhibit the biosynthesis of ergosterin in fungi.There are three main commercial products: Raxil, Folicur and Horizon.
唑醇属三唑
杀菌剂,可抑制真菌中麦角甾醇
合成,主要商品有:立克莠、富力库、菌立克三种。
By the reaction of 2 aryl 5 mercapto 1,3,4 triazoles with alkyl dihalide in presence of dilute base, ten new title compounds had been prepared.
以2-芳基-5-巯基-1,3,4-三唑为原料,在稀碱存在下与二卤代烷反应合成了10个新标题化合
。
Nitro 1,2,4 triazole 5 one(NTO)can be obtained by nitrating 1,2,4 triazole 3 one (TO) under different conditions,and nitrobenzyl derivatives of TO are prepared as well.
研究了1,2,4三唑酮3(TO)衍合成,结果表明TO在多种硝化条件下均可制得3硝基1,2,4三唑酮5(NTO),同时还合成了TO
二取代硝基苯衍
。
声明:以上例句、词性分均由互联网资源自动
成,部分未经过人工审核,其表达内容亦不代表本软件
观点;若发现问题,欢迎向我们指正。