Asymmetric Ion-Pairing Catalysis of the Reversible Cyclization of 2′-Hydroxychalcone to Flavanone: Asymmetric Catalysis of an Equilibrating Reaction

2012 ◽  
Vol 2012 (28) ◽  
pp. 5573-5584 ◽  
Author(s):  
Lukas Hintermann ◽  
Claudia Dittmer
2003 ◽  
Vol 81 (11) ◽  
pp. 1280-1284 ◽  
Author(s):  
David B Llewellyn ◽  
Bruce A Arndtsen

The chiral borate counteranion bis[(R)-1,1′-bi-2-naphtholato]borate (1–) has been found to be a competent chiral 1H NMR shift reagent for cationic copper(I) complexes. This has been demonstrated by the addition of the Cu(NCMe)4+ salt of 1– to two classes of common chiral ligands in asymmetric catalysis: 2,2′-bis(di-p-tolylphosphino)-1,1′-binaphthyl (tol-BINAP) (2) and 2,2′-isopropylidenebis(4-phenyl-2-oxazoline) (3). In the case of ligand 2, the addition of 1 equiv. of either (R,R)-2 or (S,S)-2 to Cu(NCMe)4+1– results in well-resolved 1H NMR resonances for the two enantiomers. Examination of standard solutions of non-enantiopure 2 shows that the copper complex can be an effective NMR shift reagent of a wide range of enantiomeric compositions. Cu(NCMe)4+1– also generates distinct 1H NMR resonances for the two separate enantiomers of 2,2′-isopropylidenebis(4-phenyl-2-oxazoline) (3). However, attempts to employ this copper salt as a chiral NMR shift reagent for rac-3 led to the discovery of a new and unexpected equilibrium: [(R,R)-3]Cu+ + [(S,S)-3]Cu+ [Formula: see text] [(R,R)-3][(S,S)-3]Cu+ + Cu+. Key words: chiral counteranion, copper, chiral NMR shift reagent, ion pairing.


2020 ◽  
Author(s):  
James Sterling ◽  
Wenjuan Jiang ◽  
Wesley M. Botello-Smith ◽  
Yun L. Luo

Molecular dynamics simulations of hyaluronic acid and heparin brushes are presented that show important effects of ion-pairing, water dielectric decrease, and co-ion exclusion. Results show equilibria with electroneutrality attained through screening and pairing of brush anionic charges by cations. Most surprising is the reversal of the Donnan potential that would be expected based on electrostatic Boltzmann partitioning alone. Water dielectric decrement within the brush domain is also associated with Born hydration-driven cation exclusion from the brush. We observe that the primary partition energy attracting cations to attain brush electroneutrality is the ion-pairing or salt-bridge energy associated with cation-sulfate and cation-carboxylate solvent-separated and contact ion pairs. Potassium and sodium pairing to glycosaminoglycan carboxylates and sulfates consistently show similar abundance of contact-pairing and solvent-separated pairing. In these crowded macromolecular brushes, ion-pairing, Born-hydration, and electrostatic potential energies all contribute to attain electroneutrality and should therefore contribute in mean-field models to accurately represent brush electrostatics.


2003 ◽  
Vol 7 (17) ◽  
pp. 1737-1757 ◽  
Author(s):  
A. Malkov ◽  
P. Kocovsky
Keyword(s):  

2003 ◽  
Vol 7 (17) ◽  
pp. 1759-1770 ◽  
Author(s):  
T. RajanBabu ◽  
Yuan-Yong Yan ◽  
Seunghoon Shin
Keyword(s):  

2020 ◽  
Vol 24 (20) ◽  
pp. 2341-2355
Author(s):  
Thaipparambil Aneeja ◽  
Sankaran Radhika ◽  
Mohan Neetha ◽  
Gopinathan Anilkumar

One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated reaction, ring-opening of tetrahydrofuran, triflic anhydrate mediated reaction, etc. were reported for imidazoline synthesis. This review describes an overview of the one-pot synthesis of imidazolines and covers literature up to 2020.


2019 ◽  
Vol 23 (11) ◽  
pp. 1168-1213 ◽  
Author(s):  
Samar Noreen ◽  
Ameer Fawad Zahoor ◽  
Sajjad Ahmad ◽  
Irum Shahzadi ◽  
Ali Irfan ◽  
...  

Background: Asymmetric catalysis holds a prestigious role in organic syntheses since a long time and chiral inductors such as ligands have been used to achieve the utmost desired results at this pitch. The asymmetric version of Tsuji-Trost allylation has played a crucial role in enantioselective synthesis. Various chiral ligands have been known for Pdcatalyzed Asymmetric Allylic Alkylation (AAA) reactions and exhibited excellent catalytic potential. The use of chiral ligands as asymmetric inductors has widened the scope of Tsuji-Trost allylic alkylation reactions. Conclusion: Therefore, in this review article, a variety of chiral inductors or ligands have been focused for palladium catalyzed asymmetric allylic alkylation (Tsuji-Trost allylation) and in this regard, recently reported literature (2013-2017) has been described. The use of ligands causes the induction of enantiodiscrimination to the allylated products, therefore, the syntheses of various kinds of ligands have been targeted by many research groups to employ in Pd-catalyzed AAA reactions.


2020 ◽  
Vol 09 ◽  
Author(s):  
Minita Ojha ◽  
R. K. Bansal

Background: During the last two decades, horizon of research in the field of Nitrogen Heterocyclic Carbenes (NHC) has widened remarkably. NHCs have emerged as ubiquitous species having applications in a broad range of fields, including organocatalysis and organometallic chemistry. The NHC-induced non-asymmetric catalysis has turned out to be a really fruitful area of research in recent years. Methods: By manipulating structural features and selecting appropriate substituent groups, it has been possible to control the kinetic and thermodynamic stability of a wide range of NHCs, which can be tolerant to a variety of functional groups and can be used under mild conditions. NHCs are produced by different methods, such as deprotonation of Nalkylhetrocyclic salt, transmetallation, decarboxylation and electrochemical reduction. Results: The NHCs have been used successfully as catalysts for a wide range of reactions making a large number of building blocks and other useful compounds accessible. Some of these reactions are: benzoin condensation, Stetter reaction, Michael reaction, esterification, activation of esters, activation of isocyanides, polymerization, different cycloaddition reactions, isomerization, etc. The present review includes all these examples published during the last 10 years, i.e. from 2010 till date. Conclusion: The NHCs have emerged as versatile and powerful organocatalysts in synthetic organic chemistry. They provide the synthetic strategy which does not burden the environment with metal pollutants and thus fit in the Green Chemistry.


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