Javascript must be enabled to continue!
Advances in asymmetric oxidative kinetic resolution of racemic secondary alcohols catalyzed by chiral Mn(III) salen complexes
View through CrossRef
AbstractEnantiomerically pure secondary alcohols are essential compounds in organic synthesis and are used as chiral auxiliaries and synthetic intermediates in the pharmaceutical, agrochemical, and fine chemical industries. One of the attractive and practical approaches to achieving optically pure secondary alcohols is oxidative kinetic resolution of racemic secondary alcohols using chiral Mn(III) salen complexes. In the last decade, several chiral Mn(III) salen complexes have been reported with excellent enantioselectivity and activity in the homogeneous and heterogeneous catalysis of the oxidative kinetic resolution of racemic secondary alcohols. This review article is an overview of the literature on the recent development of chiral Mn(III) salen complexes for oxidative kinetic resolution of racemic secondary alcohols. The catalytic activity of monomeric, dimeric, macrocyclic, polymeric, and silica/resin supported chiral Mn(III) salen complexes is discussed in detail.
Title: Advances in asymmetric oxidative kinetic resolution of racemic secondary alcohols catalyzed by chiral Mn(III) salen complexes
Description:
AbstractEnantiomerically pure secondary alcohols are essential compounds in organic synthesis and are used as chiral auxiliaries and synthetic intermediates in the pharmaceutical, agrochemical, and fine chemical industries.
One of the attractive and practical approaches to achieving optically pure secondary alcohols is oxidative kinetic resolution of racemic secondary alcohols using chiral Mn(III) salen complexes.
In the last decade, several chiral Mn(III) salen complexes have been reported with excellent enantioselectivity and activity in the homogeneous and heterogeneous catalysis of the oxidative kinetic resolution of racemic secondary alcohols.
This review article is an overview of the literature on the recent development of chiral Mn(III) salen complexes for oxidative kinetic resolution of racemic secondary alcohols.
The catalytic activity of monomeric, dimeric, macrocyclic, polymeric, and silica/resin supported chiral Mn(III) salen complexes is discussed in detail.
Related Results
Simultaneous hyperthermia‐chemotherapy effect by arterial injection of Fe(Salen) for femur tumor
Simultaneous hyperthermia‐chemotherapy effect by arterial injection of Fe(Salen) for femur tumor
We previously identified a novel nanomagnetic particle, N,N′‐bis(salicylidene)ethylenediamine iron [Fe(Salen)]. Fe(Salen) not only shows antitumor effects but also magnetic propert...
Advances on broadband and resonant chiral metasurfaces
Advances on broadband and resonant chiral metasurfaces
Abstract
Chirality describes mirror symmetry breaking in geometric structures or certain physical quantities. The interaction between chiral structure and chiral ...
Design, synthesis and evaluation in enantioselective catalysis of diverse adjustable axially chiral biphenyl ligands and catalysts
Design, synthesis and evaluation in enantioselective catalysis of diverse adjustable axially chiral biphenyl ligands and catalysts
Chiral compounds widely occur in biomolecules, natural products and drugs, and acquisition of chirality in the chiral molecules highly depends on chiral inducers including chiral l...
Chiral Ionic Liquids as Stationary Phases in Electrophoretic Separations
Chiral Ionic Liquids as Stationary Phases in Electrophoretic Separations
Ionic liquids (ILs) are exceptional solvents having melting points at or
below 100 0C. They are completely made up of ions, often consisting of an organic
cation and an inorganic o...
Complete assignments of NMR data of salens and their cobalt (III) complexes
Complete assignments of NMR data of salens and their cobalt (III) complexes
AbstractSalens, derived from 1,2‐ethylenediamine and salicylaldehydes, have been widely used as ligands for metal complexes which have been showing enormous potential in chemical p...
The Origin of Relative Stability of Di-µ-oxo M–M Chiral Salen Complexes [M–M = Ti(IV)–Ti(IV), V(IV)–V(IV), Cr(IV)–Cr(IV), and Mn(IV)–Mn(IV)]: A Quantum-Chemical Analysis
The Origin of Relative Stability of Di-µ-oxo M–M Chiral Salen Complexes [M–M = Ti(IV)–Ti(IV), V(IV)–V(IV), Cr(IV)–Cr(IV), and Mn(IV)–Mn(IV)]: A Quantum-Chemical Analysis
Abstract
Di-µ-oxo dimetal cores can form dinuclear complexes with definite stereochemistries. Recent studies describing the synthesis and evaluation of titanium(IV) ...
Complexes salen supportés sur rGO : catalyseurs énantiosélectifs recyclables
Complexes salen supportés sur rGO : catalyseurs énantiosélectifs recyclables
rGO-supported salen complexes as efficient and recyclable enantioselective catalysts
Les matériaux à base de carbone sont largement utilisés comme supports très sta...
A Non-enantiopure H8-BINOL Metal-Organic Framework for Enantioselective Fluorescence Sensing
A Non-enantiopure H8-BINOL Metal-Organic Framework for Enantioselective Fluorescence Sensing
A major challenge in chiral sensing technologies is the reliance on enantiopure materials to differentiate between enantiomers, as their interactions with a chiral system produce d...

