نتایج جستجو برای: organocatalyst

تعداد نتایج: 407  

Journal: :Organic & biomolecular chemistry 2006
Tian-Yu Liu Jun Long Bang-Jing Li Lin Jiang Rui Li Yong Wu Li-Sheng Ding Ying-Chun Chen

The bifunctional thiourea-tertiary amine derivatives of simple chiral diamines serve as highly enantioselective catalysts for the Michael addition of alpha-substituted cyanoacetates to vinyl sulfones, giving an efficient protocol for the construction of an all-carbon substituted quaternary stereocentre.

2013
Tatjana Heckel Dagny Dagmara Konieczna

Chitosan, which is derived from the biopolymer chitin, can be readily dissolved in different ionic liquids. The resulting homogeneous solutions were applied in an asymmetric Aldol reaction. Depending on the type of ionic liquid used, high asymmetric inductions were found. The influence of different additives was also studied. The best results were obtained in [BMIM][Br] without an additive.

Journal: :Chemical communications 2009
Zoltán Dalicsek Ferenc Pollreisz Tibor Soós

A practical, cost-saving tagging approach is developed which takes advantage of the hydrophobicity of trifluoromethyl groups, exemplified by the application and recovery of a CBS precatalyst using tuned aqueous-organic media with minimum 50% water content.

Journal: :Organic Process Research & Development 2021

Hydrogen bonding phase-transfer catalysis offers a convenient solution to activate safe and economical metal alkali fluorides for enantioselective nucleophilic fluorination. Herein, we demonstrate the scalability of this protocol with fluorination 200 g racemic trans-N,N-dibenzyl-2-bromocyclohexan-1-amine in mechanically stirred 1 L glass reactor using 0.5 mol % bis-urea organocatalyst. In thes...

Journal: :Catalysts 2021

Michael addition is one of the most important carbon–carbon bond formation reactions. In this study, an (R, R)-1,2-diphenylethylenediamine (DPEN)-based thiourea organocatalyst was applied to asymmetric nitroalkenes and cycloketones produce a chiral product. The primary amine moiety in DPEN reacts with ketone form enamine activated through hydrogen between nitro group ?, ?-unsaturated nitroalken...

Journal: :Catalysts 2022

Electrochemical synthesis has been rapidly developing over the past few years. Here, we report a practical and eco-friendly electrocatalytic isomerization of allylic alcohols to their corresponding carbonyl compounds. This reaction can be carried out in undivided cells without addition external chemical oxidants metal catalysts. Moreover, this features broad substrate scope including challengin...

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