Chiral Carboxylic Acids Research Articles

Direct Lewis Acid Catalyzed Conversion of Enantioenriched N-Acyloxazolidinones to Chiral Esters, Amides, and Acids.

The identification of Yb(OTf)3 through a multivariable high-throughput experimentation strategy has enabled a unified protocol for the direct conversion of enantioenriched N-acyloxazolidinones to the corresponding chiral esters, amides, and carboxylic acids. This straightforward and catalytic method has shown remarkable chemoselectivity for substitution at the acyclic N-acyl carbonyl for a diverse array of N-acyloxazolidinone substrates. The ionic radius of the Lewis acid catalyst was demonstrated as a key driver of catalyst performance that led to the identification of a robust and scalable esterification of a pharmaceutical intermediate using catalytic Y(OTf)3.

Enantiodivergent Desymmetrization in the Rhodium(III)-Catalyzed Annulation of Sulfoximines with Diazo Compounds.

RhIII - and IrIII -catalyzed asymmetric C-H functionalization reactions of arenes have relied on the employment of chiral RhIII /IrIII cyclopentadienyl catalysts, the introduction of chiral carboxylic acids to achiral Cp*RhX2 catalysts, and the integration of both strategies. Despite considerable progress, each reaction only provided a specific configuration of the enantioenriched product when using a particular chiral catalyst. Reported in this work is the enantiodivergent coupling of sulfoximines with various diazo compounds by RhIII -catalyzed desymmetrizing annulation. The enantiodivergence was enabled by a judicious choice of achiral carboxylic acids, and the enantioselectivity correlates with the steric bias of the carboxylic acid and the sulfoximine.

Enantiodivergent Desymmetrization in the Rhodium(III)‐Catalyzed Annulation of Sulfoximines with Diazo Compounds

AbstractRhIII‐ and IrIII‐catalyzed asymmetric C−H functionalization reactions of arenes have relied on the employment of chiral RhIII/IrIII cyclopentadienyl catalysts, the introduction of chiral carboxylic acids to achiral Cp*RhX2 catalysts, and the integration of both strategies. Despite considerable progress, each reaction only provided a specific configuration of the enantioenriched product when using a particular chiral catalyst. Reported in this work is the enantiodivergent coupling of sulfoximines with various diazo compounds by RhIII‐catalyzed desymmetrizing annulation. The enantiodivergence was enabled by a judicious choice of achiral carboxylic acids, and the enantioselectivity correlates with the steric bias of the carboxylic acid and the sulfoximine.

Enantioselective Cobalt(III)-Catalyzed C-H Activation Enabled by Chiral Carboxylic Acid Cooperation.

The enantioselective cobalt(III)-catalyzed C-H alkylation was achieved through the design of a novel chiral acid. The cobalt(III)-catalyzed enantioselective C-H activation was characterized by high position-, regio- and enantio-control under exceedingly mild reaction conditions. Thereby, the robust cooperative cobalt(III) catalysis proved tolerant of valuable electrophilic functional groups, including hydroxyl, bromo, and iodo substituents. Mechanistic studies revealed a considerable additive effect on kinetics and on a negative non-linear-effect.

Enantioselective Cobalt(III)‐Catalyzed C−H Activation Enabled by Chiral Carboxylic Acid Cooperation

AbstractThe enantioselective cobalt(III)‐catalyzed C−H alkylation was achieved through the design of a novel chiral acid. The cobalt(III)‐catalyzed enantioselective C−H activation was characterized by high position‐, regio‐ and enantio‐control under exceedingly mild reaction conditions. Thereby, the robust cooperative cobalt(III) catalysis proved tolerant of valuable electrophilic functional groups, including hydroxyl, bromo, and iodo substituents. Mechanistic studies revealed a considerable additive effect on kinetics and on a negative non‐linear‐effect.

Chiral Carboxylic Acid Enabled Achiral Rhodium(III)-Catalyzed Enantioselective C-H Functionalization.

Reported is an achiral Cpx RhIII /chiral carboxylic acid catalyzed asymmetric C-H alkylation of diarylmethanamines with a diazomalonate, followed by cyclization and decarboxylation to afford 1,4-dihydroisoquinolin-3(2H)-one. Secondary alkylamines as well as nonprotected primary alkylamines underwent the transformation with high enantioselectivities (up to 98.5:1.5 e.r.) by using a newly developed chiral carboxylic acid as the sole source of chirality to achieve enantioselective C-H cleavage by a concerted metalation-deprotonation mechanism.

Chiral Carboxylic Acid Enabled Achiral Rhodium(III)‐Catalyzed Enantioselective C−H Functionalization

AbstractReported is an achiral CpxRhIII/chiral carboxylic acid catalyzed asymmetric C−H alkylation of diarylmethanamines with a diazomalonate, followed by cyclization and decarboxylation to afford 1,4‐dihydroisoquinolin‐3(2H)‐one. Secondary alkylamines as well as nonprotected primary alkylamines underwent the transformation with high enantioselectivities (up to 98.5:1.5 e.r.) by using a newly developed chiral carboxylic acid as the sole source of chirality to achieve enantioselective C−H cleavage by a concerted metalation‐deprotonation mechanism.

Explicit Solvation of Carboxylic Acids for Vibrational Circular Dichroism Studies: Limiting the Computational Efforts without Losing Accuracy.

On the basis of a comprehensive analysis of experimental and theoretical IR and vibrational circular dichroism (VCD) spectra, we make suggestions for solvation schemes for carboxylic acids. More specifically, we have studied two chiral carboxylic acids in solvents of different polarity and hydrogen bonding capabilities and verify previously proposed solute-solvent structures for their general applicability. Explicit solvation with acetonitrile- d3 is shown to be most important for carboxylic acid groups directly attached to a stereocenter, while dimethylsulfoxide- d6 should always be considered explicitly in spectra analysis. In order to circumvent the need to consider dimerization with calculations on the full homodimer in nonpolar solvents such as chloroform- d1, we quantitatively evaluate the quality of truncated models. Methanol- d4 is concluded to be the most challenging solvent for VCD studies of carboxylic acids, as the acid strength affects the hydrogen bonding strength to methanol and thus significantly determines the degree and effect of solvation. With the help of matrix-isolation IR spectroscopy, we also characterize the monomeric species of α-phenylpropionic acid.

Pd(II)-Catalyzed Enantioselective C(sp3)-H Arylation of Free Carboxylic Acids.

A monoprotected aminoethyl amine chiral ligand based on an ethylenediamine backbone was developed to achieve Pd-catalyzed enantioselective C(sp3)-H arylation of cyclopropanecarboxylic and 2-aminoisobutyric acids without using exogenous directing groups. This new chiral catalyst affords new disconnection for preparing diverse chiral carboxylic acids from simple starting materials that are complementary to the various ring forming approaches.

A Molecular docking study to predict enantioseparation of some chiral carboxylic acid derivatives by methyl-β-cyclodextrin

A molecular docking study, using molecular mechanics calculations with Arguslab, was used to help predict the enantioseparation of some guest molecules of chiral carboxylic acid derivatives by heptakis-2,6-di-O-methyl-β-cyclodextrin (DIMEB) and heptakis-2,3,6-tri-O-methyl-β-cyclodextrin (TRIMEB) as host molecules. The small differences in the binding free energy values (ΔΔG) obtained from Arguslab did not indicate any significant enantioseparation. From the molecular docking simulation results, it is predicted that in the case of DIMEB as host molecule, R-enantiomer of Etodolac, Fenoprofen, Indoprofen, Ketorolac, and Naproxen will be eluted first than S-enantiomer; However, S-enantiomer of Carprofen, Flurbiprofen, Ketoprofen, Pirprofen, Proglumide, Sulindac, Surprofen, and Zaltoprofen will be eluted first than R-enantiomer by DIMEB as host molecule. When TRIMEB is used as a host molecule, R-enantiomer of Carprofen, Flurbiprofen, Indoprofen, Ketoprofen, Naproxen, Pirprofen, and Surprofen will be eluted first than S-enantiomer; However, S-enantiomer of Etodolac, Fenoprofen, Ketorolac, Proglumide, Sulindac and Zaltoprofen will be eluted first than R-enantiomer by TRIMEB as host molecule.

(Invited) Controlling Optical Properties of Semiconductor Nanocrystals: Chiral Quantum Dots and Luminescent Solar Concentrators

This talk will discuss two areas of research in utilizing semiconductor nanocrystals in nanophotonics. The first part of the talk will describe our recent work on chiral semiconductor nanocrystals. Chiral optical materials exhibit differential optical properties under right handed and left handed circularly polarized light, and may find application in metaphotonic devices, in spin-based systems, or as luminescent sensors. Chirality can be introduced into semiconductor nanocrystals via different routes, including from chiral ligands on the surface of the nanocrystal. However, the application of these materials in photonics is limited by the relatively low dissymmetry factors. Using post-synthetic ligand exchange, we synthesized a class of chiral CdSe nanocrystals with a variety of different chiral ligands bound to the surface. We first synthesized CdSe nanocrystals via non-hot injection methods, with native, achiral carboxylic acids on the surface. As synthesized, these nanocrystals do not exhibit any circular dichroism. Post-synthetic ligand exchange of the native ligands to chiral carboxylic acids results in circular dichroism spectra associated with the excitonic transitions of the CdSe nanocrystal. We examine a family of related carboxylic acid ligands, which reveal a 30-fold difference in dissymmetry factors, reaching as high as 7 x 10-4, and show how the structure of the ligands influences the resulting circular dichroism spectra. The second part of the talk will discuss the use of luminescent semiconductor nanocrystals in diffuse light concentrators for solar energy conversion. Luminescent solar concentrators consist of embedded luminescent materials inside a polymer waveguide, such that high energy light is absorbed by the luminophore and the emitted light is trapped within the waveguide and concentrated onto a solar cell. Efficient operation of these concentrators requires not only high quality luminescent materials, but also a photonic mirror to trap luminescent light within the concentrator. We have recently designed a series of mirrors that operate cooperatively with luminescent materials inside these concentrators, showing how the design of the mirrors changes with different luminophore properties. The top-surface mirror serves to trap luminescent light inside the concentrator that would otherwise couple to the escape cone. This light propagates at a steep angle, and is especially vulnerable to reabsorption losses before reaching the edge of the concentrator. By incorporating a metamirror into the LSC, this light can be steered toward the edge for improved collection. We show that this metamirror in turn lowers the required quantum yield; equivalent performance is achieved from a luminophore with 76% quantum yield as one in a standard design with 99% quantum yield. We then designed a series of different top mirrors for different specific properties of candidate luminophores, including Si and CdSe/CdS of varying shell thickness, showing how the luminophore and mirror can be designed cooperatively.

Visual and Colorimetric High-Throughput Analysis of Chiral Carboxylic Acids Based on Enantioselective Charge Shielding of Gold Nanoparticles.

Because chiral carboxylic acids (CCAs) are a class of important biological molecules and common functional moieties found in pharmaceutical molecules, the chiral analysis of CCAs has received much attention. Herein, we developed a simple, rapid, and cost-effective method for visual and colorimetric high-throughput analysis of CCAs using chiral di-imine structure-modified gold nanoparticles (C-AuNPs) as the probe. The C-AuNPs are positively charged in the presence of zinc ion, and they can be enantioselectively shielded by the negatively charged CCA enantiomers. Therefore, upon the addition of different concentrations and enantiomeric excess (ee) of CCAs, the C-AuNP-based sensor shows the different levels of aggregation along with the visual changes in solution color, which can achieve simultaneous analysis of the concentration and ee of CCAs. The chiral recognition mechanism based on C-AuNPs was investigated by the determination of binding constants ( K) and molecular simulation methods. Our approach is expected to have the wide-ranging applications in the developing region for enantio-sensing of various chiral drugs and biomolecules.

Highly Enantioselective Synthesis of Cyclic Aminals with a Cyclopentadiene‐Based Chiral Carboxylic Acid

A highly enantioselective aminalization of 2‐aminobenzenesulfonamides and aldehydes catalyzed by a novel cyclopentadiene‐based chiral carboxylic acid has been realized. The cost‐effective and readily synthesized cyclopentadiene‐based chiral carboxylic acid was found to be a highly reactive Brønsted acid for this transformation, affording benzothiadiazine class of cyclic aminals with up to 98 % ee.

A chiral nickel DBFOX complex as a bifunctional catalyst for visible-light-promoted asymmetric photoredox reactions.

The enantioselective photoredox reaction of α,β-unsaturated carbonyl compounds and tertiary/secondary α-silylamines was enabled by a readily available single NiII-DBFOX catalyst (DBFOX = 4,6-bis((R)-4-phenyl-4,5-dihydrooxazol-2-yl)dibenzo[b,d]furan) under visible light conditions. The non-precious chiral catalyst is involved in the photochemical process to initiate single electron transfer and at the same time provides a well-organized chiral environment for the subsequent radical transformations. Good to excellent enantioselectivities (80-99% ee) were obtained for the formation of chiral γ-amino carboxylic acid derivatives and γ-lactams.

The mechanistic promiscuity of the enzymatic esterification of chiral carboxylic acids

The studies on the enzymatic kinetic resolution of 3-phenyl-4-pentenoic acid with various trialkyl orthoesters as alkoxy group donors are presented. The obtained results indicate that enantioselectivity of presented reaction is closely related to the alkoxy group donor structure. Based on critical analysis of the literature data and our own results we found that the previously recognized mechanism of such transformation is highly unlikely. In this paper we proposed a new revised mechanism explaining the role of alkoxy group donors. For trialkyl orthobenzoates excellent enzymatic kinetic resolution of target substrate was achieved. The presented method is an unique example of an enzymatic promiscuous activity toward esterification of carboxylic acids.

Circular Dichroism of CdSe Nanocrystals Bound by Chiral Carboxylic Acids.

Chiral semiconductor nanocrystals, or quantum dots (QDs), are promising materials for applications in biological sensing, photonics, and spin-polarized devices. Many of these applications rely on large dissymmetry, or g-factors, the difference in absorbance between left- and right-handed circularly polarized light compared to the unpolarized absorbance. The majority of chiral QDs, specifically CdSe, reported to date have used thiolated amino acid ligands to introduce chirality onto the nanoparticles, but these systems have ultimately reported small g-factors of ∼2 × 10-4. In an effort to realize chiral CdSe QDs with higher g-factors and to expand the set of designer chiral semiconductor nanocrystals, we have employed chiral carboxylic acids as a distinct class of ligands for chiral CdSe nanoparticles. Through this family of chiral carboxylic acid ligands, we performed a direct comparison between carboxylate-bound and thiolate-bound chiral CdSe QDs. Spectral analysis revealed that the resulting circular dichroism shifts originate from the splitting of the exciton by the ligand-nanocrystal interaction. Subsequent examination of a series of chiral carboxylic acid ligands revealed a 30-fold range in g-factor through relatively small changes in the structure of the ligand. Finally, we showed that increasing the number of stereocenters on the ligand can further enhance the dissymmetry factors. This versatile and tunable combination of nanocrystals and ligands will inform future designs of chiral nanomaterials and their applications.

Di(1-naphthyl) methanol ester of carboxylic acids for absolute stereochemical determination.

The absolute stereochemistry of chiral carboxylic acids is determined as a di(1-naphthyl)methanol ester derivative. Computational scoring of conformations favoring either P or M helicity of the naphthyl groups, capable of exciton-coupled circular dichroic coupling, leads to a predicted stereochemistry for the derivatized carboxylic acids.

Functional Chemical Groups that May Likely Become a Source for the Synthesis of Novel Central Nervous System (CNS) Acting Drugs.

Central Nervous System (CNS) disorders are on increase perhaps due to genetic, enviromental, social and dietetic factors. Unfortunately, a large number of CNS drugs have adverse effects such as addiction, tolerance, psychological and physical dependence. In view of this, literature search was carried out with a view to identify functional chemical groups that may serve as lead molecules for synthesis of compounds that may have CNS activity. The search revealed that heterocycles that have heteroatoms such as nitrogen (N), sulphur (S) and oxygen (O) form the largest class of organic compounds. They replace carbon in a benzene ring to form pyridine. Compounds with furan, thiophene, pyrrole, pyridine, azole, imidazole, indole, purine, pyrimidine, esters, carboxylic acid, aldehyde, pyrylium, pyrone, pyrodine, barbituric acid, barbiturate, quinoline, quinolone, isoquinolone, coumarin, alkylpyridine, picoline, piperidine, diazine, carboxamide, flavonoid glycoside, oxindole, aminophenol, benzimidazole, benzoxazole, benzothiazole, and chromone chemical groups among others may have CNS effects ranging from depression passing through euphoria to convulsion. Examples of the compounds with the functional groups include but not limited to coal tar, pyridostigmine, pralidoxime, quinine, mefloquine, pyrilamine, pyronaridine, ciprofloxacin and piroxicam. A number of them can undergo keto-enol tautomerism. Chiral amines may be used for derivation of chiral carboxylic acids which are components of tautomers. Some tautomers may cause parkinsonism and Stevens Johnson syndrome.

Cooperative Effects between Chiral Cpx–Iridium(III) Catalysts and Chiral Carboxylic Acids in Enantioselective C−H Amidations of Phosphine Oxides

AbstractAn enantioselective C−H amidation of phosphine oxides by using an iridium(III) catalyst bearing an atropchiral cyclopentadienyl (Cpx) ligand is reported. A very strong cooperative effect between the chiral Cpx ligand and a phthaloyl tert‐leucine enabled the transformation. Matched–mismatched cases of the different acid enantiomers are shown. The amidated P‐chiral arylphosphine oxides are formed in yields of up to 95 % and with excellent enantioselectivities of up to 99:1 er. Enantiospecific reduction provides access to valuable P‐chiral phosphorus(III) compounds.

Cooperative Effects between Chiral Cpx -Iridium(III) Catalysts and Chiral Carboxylic Acids in Enantioselective C-H Amidations of Phosphine Oxides.

An enantioselective C-H amidation of phosphine oxides by using an iridium(III) catalyst bearing an atropchiral cyclopentadienyl (Cpx ) ligand is reported. A very strong cooperative effect between the chiral Cpx ligand and a phthaloyl tert-leucine enabled the transformation. Matched-mismatched cases of the different acid enantiomers are shown. The amidated P-chiral arylphosphine oxides are formed in yields of up to 95 % and with excellent enantioselectivities of up to 99:1 er. Enantiospecific reduction provides access to valuable P-chiral phosphorus(III) compounds.