Magnetically retrievable catalysts for asymmetric synthesis
نویسندگان
چکیده
منابع مشابه
Magnetically recoverable ruthenium catalysts in organic synthesis.
Magnetically recyclable catalysts with magnetic nanoparticles (MNPs) are becoming a major trend towards sustainable catalysts. In this area, recyclable supported ruthenium complexes and ruthenium nanoparticles occupy a key place and present great advantages compared to classic catalysts. In this micro-review, attention is focused on the fabrication of MNP-supported ruthenium catalysts and their...
متن کاملBidentate Lewis acid catalysts in asymmetric synthesis*
The chemistry of bidentate Lewis acids belongs to an unexplored field of science, and so far has been only poorly studied. This paper illustrates the design of several bidentate Al and Ti Lewis acids, and their successful application to selective organic synthesis, particularly to asymmetric synthesis. For example, a new, chiral bidentate Ti(IV) complex is successfully designed by adding commer...
متن کاملTandem Reactions Combining Biocatalysts and Chemical Catalysts for Asymmetric Synthesis
The application of biocatalysts in the synthesis of fine chemicals and medicinal compounds has grown significantly in recent years. Particularly, there is a growing interest in the development of one-pot tandem catalytic systems combining the reactivity of a chemical catalyst with the selectivity engendered by the active site of an enzyme. Such tandem catalytic systems can achieve levels of che...
متن کاملMagnetically separable phase-transfer catalysts.
Magnetic nanoparticles-supported quaternary ammonium and phosphonium salts were prepared and evaluated as phase-transfer catalysts. Some of them exhibited good activities that were comparable to that of tetra-n-butylammonium iodide. The catalysts were readily separated using an external magnet and reusable without significant loss of their catalytic efficiency.
متن کاملNucleophilic chiral amines as catalysts in asymmetric synthesis.
2.1. Kinetic Resolution of Alcohols and Amines 2987 2.2. Ketene Acylation 2995 2.3. Cycloadditions 2996 2.3.1. â-Lactone Formation 2996 2.3.2. â-Lactam Formation 2997 2.3.3. Ketene Dimerization 2999 2.4. Halogenation 3000 2.5. Baylis−Hillman Reactions 3000 2.6. Desymmetrization of Cyclic Anhydrides 3002 2.7. C-Acylation 3004 2.8. Cyanation 3004 3. Solid Phase Chemistry 3007 3.1. Solution Cataly...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Coordination Chemistry Reviews
سال: 2015
ISSN: 0010-8545
DOI: 10.1016/j.ccr.2014.12.017