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Corrosion inhibition of α,β-unsaturated carbonyl compounds on steel in acid medium 被引量:5
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作者 Gao Jiancun Weng Yongji +2 位作者 Salitanate Feng Li Yue Hong 《Petroleum Science》 SCIE CAS CSCD 2009年第2期201-207,共7页
Corrosion inhibition of three α,β-unsaturated carbonyl compounds on N80 steel at high temperature and in concentrated acid medium was evaluated, and the inhibition mechanism was investigated. The results proved that... Corrosion inhibition of three α,β-unsaturated carbonyl compounds on N80 steel at high temperature and in concentrated acid medium was evaluated, and the inhibition mechanism was investigated. The results proved that both cinnamaldehyde and benzalacetone had an evident anticorrosion effect and could reduce the corrosion of steel effectively in acid medium, α,β-unsaturated carbonyl compounds with a benzene ring structure had good adsorption on steel surface. The experiments proved that polymerization of α,β-unsaturated carbonyl compounds on the steel surface at a high temperature and in concentrated acid medium resulted in a good corrosion inhibiting effect, which was attributed to the structures of α,β-unsaturated carbonyl compounds. 展开更多
关键词 α β-unsaturated carbonyl compounds corrosion inhibitor ADSORPTION oilfield acidizing treatment
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Sulfite as the substrate of C-sulfonate metabolism ofα,β-unsaturated carbonyl containing andrographolide:analysis of sulfite in rats'intestinal tract and the reaction kinetics of andrographolide with sulfite 被引量:2
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作者 HUO Zhi-Peng FENG Xin-Chi +2 位作者 WANG Yu TIAN Yu-Ting QIU Feng 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2021年第9期706-712,共7页
One-sixth of the currently known natural products containα,β-unsaturated carbonyl groups.Our previous studies reported a rare C-sulfonate metabolic pathway.Sulfonate groups were linked to theβ-carbon ofα,β-unsatu... One-sixth of the currently known natural products containα,β-unsaturated carbonyl groups.Our previous studies reported a rare C-sulfonate metabolic pathway.Sulfonate groups were linked to theβ-carbon ofα,β-unsaturated carbonyl-based natural compounds through this pathway.However,the mechanism of this type of metabolism is still not fully understood,especially whether it is formed through enzyme-mediated biotransformation or direct sulfite addition.In this work,the enzyme-mediated and non-enzymatic pathways were studied.First,the sulfite content in rat intestine was determined by LC-MS/MS.The results showed that the amount of sulfite in rat intestinal contents was from 41.5 to 383μg·g^(-1),whereas the amount of sulfite in rat feed was lower than the lower limit of quantitation(20μg·g^(-1)).Second,the reaction kinetics of sulfite-andrographolide reactions in phosphate buffer solutions(pH 6-8)was studied.The half-lives of andrographolide ranged from minutes to hours.This was suggested that the C-sulfonate reaction of andrographolide was very fast.Third,the C-sulfonate metabolites of andrographolide were both detected when andrographolide and L-cysteine-S-conjugate andrographolide were incubated with the rat small intestine contents or sulfite,indicating that the sulfite amount in rat intestine contents was high enough to react with andrographolide,which assisted a significant portion of andrographolide metabolism.Finally,the comparison of andrographolide metabolite profiles among liver homogenate(with NADPH),liver S9(with NADPH),small intestine contents homogenate(with no NADPH),and sulfite solution incubations showed that the C-sulfonate metabolites were predominantly generated in the intestinal tract by non-enzymatic pathway.In summary,sulfite can serve as a substrate for C-sulfonate metabolism,and these results identified non-enzymatically nucleophilic addition as the potential mechanism for C-sulfonate metabolism of compounds containingα,β-unsaturated carbonyl moiety. 展开更多
关键词 SULFITE C-Sulfonate metabolites α β-unsaturated carbonyl Reaction kinetics ANDROGRAPHOLIDE Non-enzymatic
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Novel and Efficient One Pot Condensation Reactions between Ketones and Aromatic Alcohols in the Presence of CrO3 Producing α,β-Unsaturated Carbonyl Compounds
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作者 李亚男 陈道勇 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2011年第10期2086-2090,共5页
We report a new, effective and simple method for preparing a,fl-unsaturated carbonyl compounds by reacting ketones and aromatic alcohols at 56 ℃ in the presence of CrO3 (CrO3 acts as an oxidant and also a catalyst)... We report a new, effective and simple method for preparing a,fl-unsaturated carbonyl compounds by reacting ketones and aromatic alcohols at 56 ℃ in the presence of CrO3 (CrO3 acts as an oxidant and also a catalyst) for around 10 h. The condensation reactions occurred effectively among a wide combination of ketones and alcohols. The procedure is simple and the yields can be high up to 98%. And a probable mechanism is proposed. 展开更多
关键词 one pot condensation reaction KETONE ALCOHOL CRO3 α β-unsaturated carbonyl compound
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Transition Metal Free Chemoselective Reduction ofα,β-Unsaturated Ketones to Saturated Ketones Using Tosyl Hydrazide as a Hydrogen Donor
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作者 Yarabally R Girish Kanchipura R Raghavendra +2 位作者 Dasappa Nagaraja Kothanahally S Sharath Kumar Sheena Shashikanth 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2015年第2期181-184,共4页
An efficient,inexpensive and simple method for the reduction of variousα,β-unsaturated ketones to corre-sponding saturated ketones using tosyl hydrazide as a hydrogen donor in DMF using calcium oxide powder has been... An efficient,inexpensive and simple method for the reduction of variousα,β-unsaturated ketones to corre-sponding saturated ketones using tosyl hydrazide as a hydrogen donor in DMF using calcium oxide powder has been reported.A variety of enones underwent reduction without forming undesirable side products.High chemose-lectivity,broad functional group tolerance and good yields are the noteworthy features of this protocol. 展开更多
关键词 α β-unsaturated carbonyl compounds tosyl hydrazide transition metal free saturated ketones
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氧雄龙的合成 被引量:2
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作者 贺诗华 王春婷 《精细化工》 EI CAS CSCD 北大核心 2007年第11期1112-1114,共3页
以甲基表雄醇为起始原料,环保高效地合成了氧雄龙。首先采用环保的温和氧化剂2-iodoxybenzoicacid(IBX)在65~70℃,氧化甲基表雄醇直接合成α,β-不饱和羰基甾体-17α-甲基-1-睾酮;经-30~-40℃臭氧化后,用氢氧化钠溶液碱性水解得到17β... 以甲基表雄醇为起始原料,环保高效地合成了氧雄龙。首先采用环保的温和氧化剂2-iodoxybenzoicacid(IBX)在65~70℃,氧化甲基表雄醇直接合成α,β-不饱和羰基甾体-17α-甲基-1-睾酮;经-30~-40℃臭氧化后,用氢氧化钠溶液碱性水解得到17β-羟基-17α-甲基-1-氧代-1,2-开环-A-失碳-5α-雄甾-2-含氧羧酸;最后在0~10℃,经硼氢化钠碱性条件下还原后,调节pH=1~2,内酯化反应合成了目的物。3步操作的产率分别为72%、69%及86%。中间体和目的物经红外光谱、核磁共振氢谱、质谱及元素分析确证了其化学结构。 展开更多
关键词 氧雄龙 IBX α β-不饱和羰基甾体 药物
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用IBX对醋酸去氢表雄酮选择性脱氢合成3β-乙酰氧基-雄甾-Δ^(5,15)-二烯-17-酮 被引量:2
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作者 贺诗华 王春婷 《应用化学》 CAS CSCD 北大核心 2008年第8期992-994,共3页
以醋酸去氢表雄酮为起始原料,于温度为65~70℃的DMSO-甲苯混合溶剂中,反应时间为22h,利用二碘酰基苯甲酸(IBX)对醋酸去氢表雄酮的选择性脱氢简便高效地合成了曲螺酮关键中间体3β-乙酰氧基-雄甾-Δ5,15-二烯-17-酮;探讨了IBX与醋酸去氢... 以醋酸去氢表雄酮为起始原料,于温度为65~70℃的DMSO-甲苯混合溶剂中,反应时间为22h,利用二碘酰基苯甲酸(IBX)对醋酸去氢表雄酮的选择性脱氢简便高效地合成了曲螺酮关键中间体3β-乙酰氧基-雄甾-Δ5,15-二烯-17-酮;探讨了IBX与醋酸去氢表雄酮的摩尔比对目标化合物的收率影响。实验表明,在n(IBX)∶n(醋酸去氢表雄酮)=1.5∶1.0时,目标化合物的收率最佳,达到73%。目标化合物经紫外光谱、红外光谱、核磁共振氢谱、质谱及元素分析测试技术确证了其化学结构。 展开更多
关键词 醋酸去氢表雄酮 IBX β-乙酰氧基-雄甾-△^5 15-二烯-酮 α β-不饱和羰基甾体 中间体
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简便高效合成15β,16β-亚甲基-雄甾-5-烯-3β-醇-17-酮
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作者 贺诗华 《应用化学》 CAS CSCD 北大核心 2009年第4期405-408,共4页
采用对甲苯磺酸(pTsOH)和三氟乙酸(TFA)为催化剂,邻碘酰苯甲酸(IBX)为氧化剂,于40~45℃,在Tol-DMSO混合溶剂中,将醋酸去氢表雄酮选择性脱氢,简便高效地制备了3β-乙酰氧基-雄甾-5,15-二烯-17-酮(Ⅰ),产率分别为77%和89%。本合... 采用对甲苯磺酸(pTsOH)和三氟乙酸(TFA)为催化剂,邻碘酰苯甲酸(IBX)为氧化剂,于40~45℃,在Tol-DMSO混合溶剂中,将醋酸去氢表雄酮选择性脱氢,简便高效地制备了3β-乙酰氧基-雄甾-5,15-二烯-17-酮(Ⅰ),产率分别为77%和89%。本合成线路有效避免了经溴代脱溴和发酵等合成线路反应繁多、试剂毒性大、成本高以及单纯IBX选择性脱氢反应温度高、反应时间长等不足。然后将化合物Ⅰ在碱性条件下水解得到3β-羟基-雄甾-5,15-二烯-17-酮(Ⅱ),产率92%。最后将化合物Ⅱ与碘化三甲基氧化锍进行迈克尔共轭加成制得目的物15β,16β-亚甲基-雄甾-5-烯-3β-醇-17-酮(Ⅲ),产率89%。中间体和目的物经紫外光谱、红外光谱、核磁共振氢谱、质谱及元素分析确证了其化学结构。 展开更多
关键词 醋酸去氢表雄酮 IBX 15β 16β-亚甲基-雄甾烯-3β-醇酮 α β-不饱和羰基甾体 中间体
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Facile Aldol Reaction Between Unmodified Aldehydes and Ketones in Bronsted Acid Ionic Liquids 被引量:3
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作者 LIU Bao-you ZHAO Di-shun +1 位作者 XU Dan-qian XU Zhen-yuan 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2007年第5期549-553,共5页
A series of condensation reactions of unmodified ketones and aromatic aldehydes to prepare α,β-unsaturated carbonyl compounds by means of Aldol reactions in Bronsted acid ionic liquids(BAILs)was explored.1-Butyl-3... A series of condensation reactions of unmodified ketones and aromatic aldehydes to prepare α,β-unsaturated carbonyl compounds by means of Aldol reactions in Bronsted acid ionic liquids(BAILs)was explored.1-Butyl-3-methylimidazolium hydrogen sulphate(BMImHSO4)acting as an effective media and catalyst in aldol reactions was compared with other BAILs,with the advantages of high conversion and selectivity.The product was easily isolated and the left ionic liquid can be readily recovered and reused at least 3 times with almost the same efficiency.The scope and limitation of the present method were explored and the possible catalytic mechanism was speculated. 展开更多
关键词 Bronsted acid ionic liquid(BAIL) Aldol reaction α β-unsaturated carbonyl compound
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非甾体抗炎药4-(2-噻吩羰基)苯酚类化合物的抗炎活性 被引量:1
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作者 戴德哉 吴楚武 黄珺 《中国药科大学学报》 CAS CSCD 北大核心 1991年第1期44-47,共4页
非甾体类抗炎药临床上用于治疗风湿性关节炎及其它胶原性疾病。国内外正不断地寻找新的化合物。我们曾发现氨甲基酚类化合物有较好的抗炎活性。
关键词 噻吩羰基苯酚 抗炎活性 抗炎药
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响应面法优化羰基还原酶产生菌Cyberlindnera saturnus发酵培养基 被引量:7
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作者 肖美娟 朱治任 +1 位作者 刘月旺 王普 《生物加工过程》 CAS 2021年第1期47-53,共7页
(13R,17S)乙基仲醇是合成甾体类避孕药物左炔诺孕酮的手性中间体,可利用Cyberlindnera saturnus ZJPH1807菌株催化乙基二酮不对称还原制备(13R,17S)乙基仲醇。为进一步提高该菌株的羰基还原酶活力,采用单因素实验和响应面优化法对其发... (13R,17S)乙基仲醇是合成甾体类避孕药物左炔诺孕酮的手性中间体,可利用Cyberlindnera saturnus ZJPH1807菌株催化乙基二酮不对称还原制备(13R,17S)乙基仲醇。为进一步提高该菌株的羰基还原酶活力,采用单因素实验和响应面优化法对其发酵培养基中碳源、氮源及无机盐等主要成分和添加量进行优化,得到最优培养基组成(g/L):葡萄糖34.36、酵母膏14.89、NH4Cl30.34、KH2PO41.01。采用优化后的发酵培养基,菌体比酶活达0.27 U/g(以1 g细胞计),生物量为6.13 g/L,分别比优化前提高了233.33%和20.39%,为高效合成左炔诺孕酮提供了基础。 展开更多
关键词 (13R 17S)乙基仲醇 Cyberlindnera saturnus 响应面优化 羰基还原酶 甾体药物 左炔诺孕酮 绿色制造
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3-羰基-雄甾-4-烯-17β-酸的合成
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作者 罗金峰 周雪琴 +1 位作者 刘东志 杨雄文 《化学工业与工程》 CAS 2007年第5期401-403,407,共4页
以脱氢异雄酮(DHEA)为原料,经过Wittig反应、硼氢化-氧化反应、Oppenauer反应和Jone’s氧化反应合成了重要甾体中间体3-羰基-雄甾-4-烯-17β-酸,总收率达23.0%,并采用核磁、质谱和红外表征了产物结构。
关键词 脱氢异雄酮 3-羰基-雄甾-4-烯-17β-酸 甾体药物 合成
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坎利酮的简便高效合成法 被引量:1
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作者 贺诗华 《中国现代应用药学》 CAS CSCD 北大核心 2010年第1期30-32,共3页
目的简便高效合成坎利酮。方法将醋酸去氢表雄酮依次经硫叶立德环氧化,NaCH(COOEt)2内酯化,2,3-二氯-5,6-二氰基-1,4-苯醌选择性脱氢得到目标产物坎利酮。结果总产率69.8%。目标物经紫外光谱、红外光谱、核磁共振氢谱、质谱及元素分析... 目的简便高效合成坎利酮。方法将醋酸去氢表雄酮依次经硫叶立德环氧化,NaCH(COOEt)2内酯化,2,3-二氯-5,6-二氰基-1,4-苯醌选择性脱氢得到目标产物坎利酮。结果总产率69.8%。目标物经紫外光谱、红外光谱、核磁共振氢谱、质谱及元素分析确证了其化学结构。结论改进后的工艺原材料价廉易得,操作简便,降低了生产成本,更适合工业化生产。 展开更多
关键词 醋酸去氢表雄酮 2 3-二氯-5 6-二氰基-1 4-苯醌 坎利酮 α β-不饱和羰基甾体 螺环羧内酯
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A clean and efficient cyclocondensation to pyrido[2,3-d]pyrimidine derivatives in aqueous media 被引量:2
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作者 Robabeh Baharfar Razieh Azimi 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第10期1183-1186,共4页
A series of pyrido[2,3-d]pyrimidine derivatives were easily constructed by cyclocondensation reactions of 6-aminouracils or 6- aminothiouracil withα,β-unsaturated carbonyl compounds(aldehyde,ketone and ester) poss... A series of pyrido[2,3-d]pyrimidine derivatives were easily constructed by cyclocondensation reactions of 6-aminouracils or 6- aminothiouracil withα,β-unsaturated carbonyl compounds(aldehyde,ketone and ester) possessing a leaving group on theβposition,in H_2O under reflux conditions. 展开更多
关键词 Pyrido[2 3-d]pyrimidine 6-Aminothiouracil Diethyl ethoxymethylenemalonate α β-unsaturated carbonyl compounds
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