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Asymmetric Double Michael Reaction Catalyzed by Simple Primary Amine Catalysts: A Straightforward Approach to Construct Spirocyclic Oxindoles 被引量:2
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作者 罗西娅 汪亮亮 +6 位作者 彭林 摆建飞 贾利娜 贺光云 田芳 徐小英 王立新 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2012年第5期1185-1188,共4页
The enantioselective double Michael reaction of N-Boc-3-nonsubstitued oxindoles with dienones catalyzed by chiral monoimide protected cyclohexane-1,2-diamines was developed. A wide range of optically active spirocycli... The enantioselective double Michael reaction of N-Boc-3-nonsubstitued oxindoles with dienones catalyzed by chiral monoimide protected cyclohexane-1,2-diamines was developed. A wide range of optically active spirocyclic oxindoles were obtained up to 98% yield and up to 89% ee. 展开更多
关键词 double Michael reaction spirocyclic oxindole amine catalyst ORGANOCATALYSIS
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Highly Selective Gas-phase Synthesis of 1,1-Dichloroethylene from 1,1,2-Trichloroethane over Supported Amine Catalysts 被引量:2
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作者 TANG Cen JIN Yanxia +4 位作者 WANG Xiaoxia HU Gengshen XIE Guanqun LI Xiaonian LUO Mengfei 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2015年第5期787-791,共5页
The manufacture of 1,1-dichloroethylene(1,1-DCE) usually employs liquid phase method to perform the dehydrochlorination of 1,1,2-trichloroethane(TCE), where large amounts of high-concentration salty wastewater is ... The manufacture of 1,1-dichloroethylene(1,1-DCE) usually employs liquid phase method to perform the dehydrochlorination of 1,1,2-trichloroethane(TCE), where large amounts of high-concentration salty wastewater is produced inevitably. It has been a long-term goal to achieve the gas phase synthesis of 1,1-DCE via supported cata- lysts. In this work, the gas-phase synthesis of 1,1-DCE from TCE was studied in the presence of pentaethylenehexamine(PEHA) supported on silica. High and stable selectivity to 1,1-DCE(up to 98%) was obtained, which could be ascribed to the relatively strong basicity of PEHA according to a proposed E2 mechanism. The formation of PEHA chloride from the HCI generated in situ was detected and was considered to be the main reason for the deactivation of PEHA catalyst. 展开更多
关键词 1 1-Dichloroethene Supported amine catalyst DEHYDROCHLORINATION
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Successive Free-Radical C(sp^(2))-C(sp^(2)) Coupling Reactions to Form Graphene 被引量:2
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作者 Huaqiang Cao Cheng Wang +6 位作者 Baojun Li Tianyu Chen Peng Han Yan Zhang Haijun Yang Qunyang Li Anthony K.Cheetham 《CCS Chemistry》 CAS 2022年第2期584-597,共14页
Graphene is of great interest because of its exciting properties and potential applications,but its production on a large-scale still presents considerable challenges.Herein,we report the synthesis of predominately fe... Graphene is of great interest because of its exciting properties and potential applications,but its production on a large-scale still presents considerable challenges.Herein,we report the synthesis of predominately few-layer graphene,due toπ–πstacking,and single-layer graphene from reaction between hexabromobenzene and Na metal,followed by annealing to improve crystallinity.The reaction proceeds via a free-radical C(sp^(2))–C(sp^(2))coupling mechanism,which is supported by theoretical calculations.The graphene can host unpaired spin electrons,leading to a short acquisition time for a solidstate nuclear magnetic resonance 13C spectrum from unlabeled graphene,which is ascribed to the very short spin-lattice relaxation time.High catalytic activity for transforming amine to imine with a conversion of>99%and a yield of∼97%is demonstrated,and high electronic conductivity of∼105 S·m^(−1) is found by terahertz spectroscopy.The reaction delivers a method for synthesizing graphene with a high spin concentration from perbrominated benzene molecules by using an active metallic agent,such as Na,Li,or Mg. 展开更多
关键词 graphene synthesis radical C(sp^(2))-C(sp^(2))coupling high electron spin density short spin-lattice relaxation metal-free amine conversion catalyst
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Efficient Synthesis of a-Amino Acid Derivatives via Phase-transfer-catalyzed Directed Reductive Amination
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作者 ZHANG Xiaohua YE Wenjing WANG Kuanglei TIAN Yongshou XIAO Xiao 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2015年第2期203-207,共5页
An efficient phase-transfer-catalyzed directed reductive amination of α-keto esters was described using simple substituted benzyl amines as nitrogen source and K2CO3 as base at room temperature, giving a series of al... An efficient phase-transfer-catalyzed directed reductive amination of α-keto esters was described using simple substituted benzyl amines as nitrogen source and K2CO3 as base at room temperature, giving a series of aliphatic a-amino acid derivatives in moderate to high yields(up to 99%). Preliminary study on this asymmetric process showed that cinchona-derived phase transfer catalyst was elTective, aflbrding the corresponding product in 13% e.e. and 40% yield. 展开更多
关键词 Direcled reductive amination: α-Amino acid: Phase transfer catalyst
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