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三唑醇化合物的
真菌活性。
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三唑醇化合物的
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
、
生素
等全身用
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
杀菌剂,可抑制真菌中麦角甾醇的生物合
,
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,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
了TO的二取代硝基苯衍生物。
声明:以上例句、词性分均由互联网资源自动生
,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,
稀
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,结果表明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.
研究具有环丙基三唑醇类化合物
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.
介绍咪唑类、三唑类、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.
唑醇属三唑类杀菌剂,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,
碱存
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1,2,4三唑酮3(TO)衍生物合成,
果表明TO
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.
研究具有环丙基结构的三唑醇类化合物的抗真活
。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
咪唑类、三唑类、烯丙胺类、抗生素类等全身用抗真
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
剂,可抑制真
中麦角甾醇的生物合成,主要商品有:
克莠、富力
、
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,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的二取代硝基苯衍生物。
声明:以上例句、词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
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、唑类、烯丙胺类、抗生素类等全身
抗真菌药的研发进展及市场
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
唑类杀菌剂,可抑制真菌中麦角甾
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
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
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-芳基-5-巯基-1,3,4-三唑为原料,稀碱
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,结果表明TO多种硝化条件
均可制得3硝基1,2,4三唑酮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三唑醇类化合物的抗真。
OBJECTIVE: To introduce the research and development of systematic antifungal drugs such as imidazole,triazole,allylamine,antibiotic etc.and the marketing trend.
绍咪唑类、三唑类、烯丙胺类、抗生素类等全身用抗真
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
剂,可抑制真
中麦角甾醇的生物合成,主要商品有:
莠、富力库、
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,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的二取代硝基苯衍生物。
声明:以上例句、词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.
介绍咪类、
类、烯丙胺类、抗生素类等全身
抗真菌药的研发进展及市
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
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-为原料,在稀碱存在下与二卤代烷反
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
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;若发现问题,欢迎向我们指正。