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Stereoselective Aldol Reaction in Aqueous Solution Using Prolinamido-Glycosides as Water-Compatible Organocatalyst
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作者 Daisuke Miura Tomoya Machinami 《Modern Research in Catalysis》 2015年第1期20-27,共8页
Prolinamido-glycoside catalyzed asymmetric aldol reaction in aqueous media is reported. The reactions are rapid and highly stereoselective when water is used as solvent. The stereoselectivities were under influence of... Prolinamido-glycoside catalyzed asymmetric aldol reaction in aqueous media is reported. The reactions are rapid and highly stereoselective when water is used as solvent. The stereoselectivities were under influence of configurations of a prolyl residue of the catalyst and α-chiral aldehydes. Water soluble prolinamido-glycoside catalysts are easily separable from reaction mixture and can be recycled and re-used several times. 展开更多
关键词 ORGANOCATALYST ALDOL Reaction Carbohydrate water-compatible PROLINAMIDE
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The Development of Molecularly Imprinted Polymers in the Clean-Up of Water Pollutants: A Review 被引量:1
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作者 Kwabena Agyarko Sarpong Wanzhen Xu +1 位作者 Weihong Huang Wenming Yang 《American Journal of Analytical Chemistry》 2019年第5期202-226,共25页
In the last decades, the extensive use of chemical and biological materials has not only seen to an increased transport of environmental pollutants but also, it has interfered and compromised the pristine state of dif... In the last decades, the extensive use of chemical and biological materials has not only seen to an increased transport of environmental pollutants but also, it has interfered and compromised the pristine state of different environmental matrices with emphasis on waterbodies. This has stimulated studies to develop and adopt novel techniques which consider the removal of pollutants with premium on economic feasibility, simple instrumentation, and high performance. In the treatment of water, the removal of trace concentration organic compounds and other numerous polluted water effluents is difficult due to limited affinity of trace compound ions to ion exchange resins. Because of the selective nature;recognition properties;adsorption ability;high stability;and easier preparation of molecular imprints, they are considered attractive and suitable artificial receptors to be applied in analytical separations, drug delivery, and as chemical sensors. In this review, we touch on the fundamentals of molecularly imprinted technologies and underscore some recent advances made in the development of imprinted polymers that are compatible with water and how they can be used in the clean-up of pollutants. The paper finally presents a comprehensive report on some challenges and outlook in the use of MIPs as water treatment sorbent. 展开更多
关键词 WASTEWATER Treatment AQUEOUS Conditions Molecularly Imprinted POLYMERS water-compatible
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Organocatalytic Stereoselective Synthesis of 3-Alkyl-3-hydroxy-2-oxindoles Catalyzed by Novel Water-compatible Axially Unfixed Biaryl-based Bifunctional Organocatalysts 被引量:1
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作者 Hongwu Zhao Wei Meng +7 位作者 Zhao Yang Ting Tian Zhihui Sheng Hailong Li Xiuqing Song Yutong Zhang Sen Yang Bo Li 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2014年第5期417-428,共12页
In this work,six novel axially unfixed biaryl-based water-compatible bifunctional organocatalysts were de-signed and synthesized for the organocatalytic access to a variety of 3-alkyl-3-hydroxy-2-oxindole derivatives ... In this work,six novel axially unfixed biaryl-based water-compatible bifunctional organocatalysts were de-signed and synthesized for the organocatalytic access to a variety of 3-alkyl-3-hydroxy-2-oxindole derivatives via aldol reactions in water.Organocatalyzed by 5a,the direct aldol reactions of isatins with enolisable ketones under-went readily in water,furnishing the structurally diverse 3-alkyl-3-hydroxy-2-oxindoles in various stereoselectivi-ties(up to>99%dr and>99%ee).Moreover,a plausible transition state of the conducted aldol reactions was hy-pothesized to shed light on the observed stereoselectivities of the obtained 3-alkyl-3-hydroxy-2-oxindoles. 展开更多
关键词 organocatalysis 3-alkyl-3-hydroxy-2-oxindole water-compatibility bifunctionality
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