Phosphine ligand and enantiomer or racemic body thereof and preparation methods thereof
A technology of enantiomers and phosphine ligands, which is applied in the field of phosphine ligands or their enantiomers or their racemates and their preparation, and can solve the problems of insufficient number and types of ligands, single skeleton space structure, etc.
Active Publication Date: 2012-07-04
SUN YAT SEN UNIV
View PDF2 Cites 18 Cited by
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
However, compared with BINAP-like bidentate phosphine ligands, the number and types of such ligands are insufficient, and the skeleton (mostly binaphthyls) and spatial structure are relatively single
Method used
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View moreExamples
Experimental program
Comparison scheme
Effect test
Embodiment 1
Embodiment 2
Embodiment 3
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More PUM
Login to View More
Abstract
The invention discloses a phosphine ligand and an enantiomer or a racemic body thereof and preparation methods and applications thereof. The structural formulae of the phosphine ligand and the enantiomer or the racemic body are shown in the specifications; a phosphine ligand compound has a novel framework; complete transfer of planar chirality to axial chirality in a synthesis process is realized through a desymmetrization reaction; a synthesis method is simple and economical; during preparation of a chiral ligand, common complex chiral splitting processes are avoided; and an obtained chiral ligand has the advantages of high reaction activity, high enantioselectivity and the like in a model reaction, can be applied to catalytic reactions of a plurality of metals such as palladium, rhodium, nickel, copper, iridium, ruthenium, iron, cobalt, gold, platinum and the like, and can have a very good catalytic effect.
Description
technical field The invention belongs to the field of chemical catalysis, and specifically relates to a class of phosphine ligands or their enantiomers or their racemates and a preparation method thereof. Background technique In asymmetric reactions, the design and synthesis of chiral catalysts with high enantioselectivity and catalytic activity are key. The design and synthesis of chiral catalysts is actually mainly the design and synthesis of chiral ligands, because they play a decisive role in the reactivity and enantioselectivity in transition metal-catalyzed asymmetric reactions [Noyori, R.; Ohkuma, T.Angew.Chem.Int.Ed.2002, 41, 2008], it can be said that the development of asymmetric catalysts is mainly reflected in the development of chiral ligands. From the perspective of chiral elements, there are central chirality, planar chirality, axial chirality and spiral chirality, etc.; from the number of coordination atoms, they can be divided into single-dentate, double-de...
Claims
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More Application Information
Patent Timeline
Login to View More
IPC IPC(8): C07F9/655C07D321/00C07D321/12B01J31/24C07F9/40C07F9/6561C07D493/04C07F9/50C07D307/33
Inventor 邱立勤吴文浩
Owner SUN YAT SEN UNIV
Who we serve
- R&D Engineer
- R&D Manager
- IP Professional
Why Eureka
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Social media
Eureka Blog
Learn More Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com