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无溶剂条件下代硫醇试剂与α,β-不饱和酮的迈克尔加成反应 被引量:7
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作者 欧阳艳 于海丰 +1 位作者 董德文 刘群 《东北师大学报(自然科学版)》 CAS CSCD 北大核心 2006年第1期67-71,共5页
用4,4-二烷硫基-3-烯-2-丁酮(1)作为无气味硫醇替代试剂在硫杂迈克尔加成反应中进行了研究.用浓盐酸做催化剂,将一系列α,β-不饱和酮(2)与1在无溶剂条件下混合发生反应,得到了相应的产率较高硫杂迈克尔加成产物(3),并对其反应机理进行... 用4,4-二烷硫基-3-烯-2-丁酮(1)作为无气味硫醇替代试剂在硫杂迈克尔加成反应中进行了研究.用浓盐酸做催化剂,将一系列α,β-不饱和酮(2)与1在无溶剂条件下混合发生反应,得到了相应的产率较高硫杂迈克尔加成产物(3),并对其反应机理进行了探讨. 展开更多
关键词 二硫缩烯酮 代硫醇试剂 硫杂迈克尔加成 Α Β-不饱和酮 无溶剂
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α,α-二乙酰基二硫缩烯酮与α,β-不饱和酮的加成反应研究
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作者 尹彦冰 姜海燕 +3 位作者 马洁 张宏波 殷春婧 李莎莎 《化学研究与应用》 CAS CSCD 北大核心 2010年第4期492-494,共3页
α,α-diacetyl ketene thioacetals had been investigated as odorless thiol equivalents in thia-Michael addition reaction.Under solvent-free conditions,a series of reactions between α,α-diacetyl ketene thioacetals and... α,α-diacetyl ketene thioacetals had been investigated as odorless thiol equivalents in thia-Michael addition reaction.Under solvent-free conditions,a series of reactions between α,α-diacetyl ketene thioacetals and α,β-unsaturated ketones were carried out promoting by concentrated hydrochloric acid.The corresponding thia-Michael adducts in high yields were obtained.Furthermore,a mechanism for this thia-Michael addition reaction was proposed preliminary. 展开更多
关键词 二硫缩烯酮 Α Β-不饱和酮 迈克尔加成反应
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Bi(OTf)3催化乙烯基硫醚对邻亚甲基苯醌的硫杂迈克尔加成反应合成邻羟基苄硫醚衍生物
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作者 石新华 彭丹 +7 位作者 王峰 牟秋红 李金辉 于一涛 赵宁 李冰 张硕 刘琳 《山东科学》 CAS 2020年第6期55-63,共9页
以2-[羟基(苯基)甲基]苯酚类化合物和乙烯基硫醚为原料,1,2-二氯乙烷为溶剂,在Bi(OTf)3催化下原位生成邻亚甲基苯醌,而后与乙烯基硫醚发生选择性硫杂迈克尔加成反应构建邻羟基苄硫醚。该反应在30℃下搅拌3 h即可完成,目标产物收率78%~88... 以2-[羟基(苯基)甲基]苯酚类化合物和乙烯基硫醚为原料,1,2-二氯乙烷为溶剂,在Bi(OTf)3催化下原位生成邻亚甲基苯醌,而后与乙烯基硫醚发生选择性硫杂迈克尔加成反应构建邻羟基苄硫醚。该反应在30℃下搅拌3 h即可完成,目标产物收率78%~88%。该反应化学选择性好,底物适用范围广,底物中2-[羟基(苯基)甲基]苯酚类化合物苯环上具有不同吸电子和给电子取代基,对于苯基乙烯基硫醚和乙基乙烯基硫醚,该反应均可以顺利得到相应产物,并且可放大至克级规模反应。 展开更多
关键词 邻亚甲基苯醌 硫杂迈克尔加成反应 Bi(OTf)3 乙烯基硫醚 邻羟基苄硫醇
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A mild and highly efficient one-pot three-component reaction for carbon-sulfur bond formation catalyzed by potassium tert-butoxide 被引量:1
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作者 Barahman Movassagh Amir Rakhshani 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第10期1179-1182,共4页
Potassium tert-butoxide has been found to be a highly efficient catalyst for one-pot,three-component reaction of aryl aldehydes, acetophenones,and thiols via Claisen-Schmidt/Michael addition reactions for the synthesi... Potassium tert-butoxide has been found to be a highly efficient catalyst for one-pot,three-component reaction of aryl aldehydes, acetophenones,and thiols via Claisen-Schmidt/Michael addition reactions for the synthesis of thia-Michael adducts in high yields. The reactions are best carried out in tert-butyl alcohol at room temperature. 展开更多
关键词 Potassium tert-butoxide thia-michael adduct Three-component reaction C-S bond formation THIOLS
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Improved “cure on demand” of aromatic bismaleimide with thiol triggered by retro-Diels-Alder reaction
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作者 Vincent Froidevaux Melanie Decostanzi +3 位作者 Abdelatif Manseri Sylvain Caillol Bernard Boutevin Remi Auvergne 《Frontiers of Chemical Science and Engineering》 SCIE EI CAS CSCD 2021年第2期330-339,共10页
This study focuses on the synthesis of new liquid aromatic bismaleimide monomers in order to improve self-curing on demand(SCOD)systems previously based on aliphatic bismaleimides.These SCOD systems are based on Diels... This study focuses on the synthesis of new liquid aromatic bismaleimide monomers in order to improve self-curing on demand(SCOD)systems previously based on aliphatic bismaleimides.These SCOD systems are based on Diels-Alder(DA)/retro-DA reactions.The syntheses of new different aromatic bismaleimides with ester and amide bonds are presented.These maleimides have been protected using DA reaction and characterized by 1H NMR analysis to determine protection rate and diastereomer ratios.The retro-DA reactions of both aromatic and aliphatic DA adducts in presence of thiol molecules were studied.Kinetic analysis was monitored by 1H NMR and compared to model study.Finally,both aromatic and aliphatic bismaleimides-based polymers were synthesized with 2-mercaptoethyl ether and thermal properties of polymers were compared.The glass transition temperature values ranged from–20°C to 14°C and very good thermal stabilities were observed(up to 300°C). 展开更多
关键词 thiol-ene polymerization self-curing on demand thia-michael addition DIELS-ALDER MALEIMIDE
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AlCl_(3)@MNPs催化硫杂Michael加成串联反应研究
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作者 应安国 白林盛 +3 位作者 侯海亮 许松林 鲁小彤 王丽敏 《有机化学》 SCIE CAS CSCD 北大核心 2022年第11期3843-3852,共10页
利用化学共沉淀法制备了超顺磁性Fe_(3)O_(4)纳米颗粒,然后在碱性环境中水解正硅酸四乙酯得到二氧化硅包覆的核壳结构(MNPs),进一步负载Al Cl_(3)得到非均相催化剂Al Cl_(3)@MNPs.采用X射线电子能谱、X射线衍射、透射电镜、扫描电镜及... 利用化学共沉淀法制备了超顺磁性Fe_(3)O_(4)纳米颗粒,然后在碱性环境中水解正硅酸四乙酯得到二氧化硅包覆的核壳结构(MNPs),进一步负载Al Cl_(3)得到非均相催化剂Al Cl_(3)@MNPs.采用X射线电子能谱、X射线衍射、透射电镜、扫描电镜及磁滞回线测试等手段对Al Cl_(3)@MNPs的物化性能和结构进行表征,表明氯化铝通过与载体表面弱配位键的形成成功负载到磁性纳米粒上.将得到的超顺磁性纳米粒负载的氯化铝(AlCl_(3)@MNPs)应用到硫杂Michael加成串联反应中.研究发现,该催化剂能有效促进胺、二硫化碳和α,β-不饱和羰基化合物加成反应,产品收率为59%~99%.催化剂具备的超顺磁性纳米颗粒的大表面积、反应时的良好分散性和Al Cl_(3)与载体表面羟基的配位作用保证了其高催化活性.另外,由于Al Cl_(3)@MNPs的超顺磁性,在外加磁场存在条件下可以简便回收,并重复使用10次,其催化效果未见大幅下降,明显优于未负载Al Cl_(3)母体,这显示了其良好的工业化应用前景. 展开更多
关键词 超顺磁性纳米颗粒 硫杂Michael加成 重复使用性 绿色化学
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