Axial Chirality Research Articles

Construction of Axially Chiral 4-Aminoquinolines by Cycloaddition and Central-to-Axial Chirality Conversion.

A two-step strategy has been established for the enantioselective synthesis of 4-aminoquinolines possessing axial chirality. This approach involves a chiral phosphoric acid-catalyzed cycloaddition, followed by a DDQ oxidation step. The method offers efficient access to a variety of 1,1'-biaryl-2,2'-amino alcohol derivatives in excellent yields and enantioselectivities (up to 98% yield and 93% ee). Furthermore, the synthetic transformation of the products was also investigated.

Remote Enantioselective ϵ-Alkylation of Copper Ethynylallenylidenes: Precise Control of Central and Axial Chirality.

Chiral tetrasubstituted allenes have emerged as important architectures for engineering biologically active compounds. The construction of unique tetrasubstituted allene scaffolds with precise control of continuous central and axial chirality remains yet to be developed. Here, we report a remote enantioselective ϵ-alkylation of yne-propargylic acetates with enals enabled by NHC and copper cooperative catalysis, leading to a series of tetrasubstituted allenes with excellent enantioselectivities (up to >99 % ee) and diastereoselectivities (up to >95 : 5 dr). This method features high regioselectivity and simultaneous control of axial and central chirality. Mechanistic studies suggest a cooperative activation mode and synergistic control of distal chirality created from the copper ethynylallenylidenes.

Remote Enantioselective ϵ‐Alkylation of Copper Ethynylallenylidenes: Precise Control of Central and Axial Chirality

AbstractChiral tetrasubstituted allenes have emerged as important architectures for engineering biologically active compounds. The construction of unique tetrasubstituted allene scaffolds with precise control of continuous central and axial chirality remains yet to be developed. Here, we report a remote enantioselective ϵ‐alkylation of yne‐propargylic acetates with enals enabled by NHC and copper cooperative catalysis, leading to a series of tetrasubstituted allenes with excellent enantioselectivities (up to >99 % ee) and diastereoselectivities (up to >95 : 5 dr). This method features high regioselectivity and simultaneous control of axial and central chirality. Mechanistic studies suggest a cooperative activation mode and synergistic control of distal chirality created from the copper ethynylallenylidenes.

Catalytic Enantioselective Functionalization of Maleimides: An Update

Comprehensive SummaryMaleimide derivatives are well‐established reactive intermediates also found in natural products, synthetic pharmaceuticals and functional polymers. Their specific reactivity found widespread applications in the field of bioconjugation and allowed for the development of highly selective functionalizations based on simple additions and cycloadditions with the possible control of central and C–N axial chirality. These multisite‐reactive scaffolds have aroused a long‐standing interest throughout the scientific community more particularly as powerful electrophilic partners and more recently as nucleophilic partners in some specific transformations. The persistent interest in these easily accessible synthetic platforms over the last decade has enabled the development of new enantioselective transformations and the major advancements in this field are presented in this review. Key Scientists

Surface Magnetic Stabilization and the Photoemission Chiral-Induced Spin-Selectivity Effect.

The spinterface mechanism was suggested as a possible origin for the chirality-induced spin-selectivity (CISS) effect and was used to explain and reproduce, with remarkable accuracy, experimental data from transport experiments showing the CISS effect. Here, we apply the spinterface mechanism to explain the appearance of magnetization at the interface between nonmagnetic metals and chiral molecules, through the stabilization of otherwise fluctuating magnetic moments. We show that the stabilization of surface magnetic moments occurs for a wide range of realistic parameters and is robust against dephasing. Importantly, we show that the direction of the surface magnetic moments is determined by the chiral axis of the chiral molecules. Armed with the concept of stable surface magnetic moments, we then formulated a theory for the photoemission CISS effect. The theory, based on spin-dependent scattering, leads to direct predictions regarding the relation between the photoemission CISS effect, the chiral axis direction, the spinterface "size", and the tilt angle of the detector with respect to the surface. These predictions are within reach of current experimental capabilities and may shed new light on the origin of the CISS effect.

Helical-Sense Matching Facilitates Supramolecular Copolymerization of Helical-Chiral Pillar[5]arenes.

Supramolecular polymerization using two-dimensional π-conjugated chiral monomers has been mainly demonstrated because the supramolecular polymerization can be controlled by stereocommunication through π-π stacking between the two-dimensional chiral monomers. We herein report supramolecular copolymerization utilizing three-dimensional pentahedrons with twisted helical chirality through different combinations of helical-chiral acidic and basic pillar[5]arenes as comonomers. In this case, helical-sense matching is key to facilitating the supramolecular copolymerization. Based on the unique helical chirality of the three-dimensional pillared structure of the pillar[5]arenes and alternate ion-pairing interactions between acidic and basic groups on their bilateral rims, the homochiral helical-sense matching system forms kinetically stable nanowire-shaped supramolecular copolymers, generating the supramolecular gel in high concentrations. At elevated temperatures, the nanowire structure undergoes a transformation into thermodynamically stable nanoparticles, resulting in a gel-to-sol transition. This process can be hindered by introducing linear guest molecules, which prohibit the unit swing of pillar[5]arenes and stabilize the nanowires and supramolecular gel. By tailoring the enantiomeric ratio (e.r.) values of the chiral combinations, the helical-sense-dependent gel-to-sol transition was realized, specifically by decreasing the e.r. values. Because of helical-sense mismatching, the heterochiral system generates short, branched nanowires and presents as a turbid solution. These distinct differences reveal that the helical-sense matching between three-dimensional chiral pillar[5]arene comonomers is important for supramolecular copolymerization.

Nickel-Catalyzed Atroposelective Carbo-Carboxylation of Alkynes with CO2: En Route to Axially Chiral Carboxylic Acids.

Precise synthesis of carboxylic acids via catalytic carboxylation with CO2 is highly appealing. Although considerable advancements have been achieved in difunctionalizing carboxylation of unsaturated hydrocarbons, the asymmetric variants are conspicuously underdeveloped, particularly in addressing axially chiral alkenes. Herein, we report the first catalytic atroposelective carboxylation of alkynes with CO2. A variety of valuable axially chiral carboxylic acids are obtained with good yields and high chemo-, regio-, E/Z and enantio-selectivities. Notably, an unexpected anti-selective carbo-carboxylation is observed in the sp2-hybrid carbo-electrophile-initiated reductive carboxylation of alkynes. Mechanistic studies including DFT calculation elucidate the origin of chiral induction and anti-selectivity in vinyl-carboxylation of alkynes.

A Multiresponsive Ferrocene‐Based Chiral Overcrowded Alkene Twisting Liquid Crystals

AbstractThe reversible modulation of chirality has gained significant attention not only for fundamental stereochemical studies but also for numerous applications ranging from liquid crystals (LCs) to molecular motors and machines. This requires the construction of switchable molecules with (multiple) chiral elements in a highly enantioselective manner, which is often a significant synthetic challenge. Here, we show that the dimerization of an easily accessible enantiopure planar chiral ferrocene‐indanone building block affords a multi‐stimuli‐responsive dimer (FcD) with pre‐determined double bond geometry, helical chirality, and relative orientation of the two ferrocene motifs in high yield. This intrinsically planar chiral switch can not only undergo thermal or photochemical E/Z isomerization but can also be reversibly and quantitatively oxidized to both a monocationic and a dicationic state which is associated with significant changes in its (chir)optical properties. Specifically, FcD acts as a chiral dopant for cholesteric LCs with a helical twisting power (HTP) of 13 μm−1 which, upon oxidation, drops to near zero, resulting in an unprecedently large redox‐tuning of the LC reflection color by up to 84 nm. Due to the straightforward stereoselective synthesis, FcD, and related chiral switches, are envisioned to be powerful building blocks for multi‐stimuli‐responsive molecular machines and in LC‐based materials.

Nickel‐Catalyzed Atroposelective Carbo‐Carboxylation of Alkynes with CO2: En Route to Axially Chiral Carboxylic Acids

Nickel‐Catalyzed Atroposelective Carbo‐Carboxylation of Alkynes with CO2: En Route to Axially Chiral Carboxylic Acids

Asymmetric Synthesis of Chiral Calix[4]arenes with Both Inherent and Axial Chirality via Cobalt‐Catalyzed Enantioselective Intermolecular C−H Annulation

AbstractInherently chiral calixarenes have garnered significant attention due to their distinctive properties, yet the development of efficient catalytic asymmetric synthesis methods remains a critical challenge. Herein, we report the asymmetric synthesis of calix[4]arenes featuring inherent or both inherent and axial chirality via a cobalt‐catalyzed C−H activation/annulation strategy in high yield with excellent enantio‐ and diastereoselectivity (up to >99 % ee and >20 : 1 dr). Electrooxidation was also suitable for this transformation to obviate the sacrificial metal oxidants, underscoring the environmentally friendly potential of this approach. A key octahedral cobaltacycle intermediate was synthesized and characterized, providing valuable insights into the mode of enantio‐ and diastereocontrol of this protocol. Noteworthy photoluminescence quantum yields of up to 0.94 were measured, underscoring the potential of these compounds in the domain of organic fluorescent materials.

Three-Level Chirality Transfer and Amplification in Liquid Crystal Supramolecular Assembly for Achieving Full-Color and White Circularly Polarized Luminescence.

Chiral liquid crystal supramolecular assembly provides an ideal strategy for constructing excellent circularly polarized luminescence (CPL) materials. However, the chirality transfer in chiral liquid crystals normally occurs at two levels from the configurational chirality to the supramolecular phase chirality. The more precise and more levels of chirality transmission are fascinating but remain challenging. The present work reports the first success of three-level chirality transfer and amplification from configurationally point chirality of small molecules to conformationally helical chirality of helical polymers and finally to supramolecular phase chirality of cholesteric liquid crystals composed of chiral nonfluorescent polymers (P46) and nematic liquid crystals. Noticeably, the helical twisting power of P46 is five-fold larger than its monomer. Full-color and white CPL with maximum luminescence dissymmetry factor up to 1.54 and photoluminescence quantum yield up to 63.8% are realized utilizing helical supramolecular assembly combined with selective reflection mechanism. Also significantly, the electrically stimuli-responsive CPL switching device as well as anti-counterfeiting security, information encryption, and chiral logic gate applications are developed. This study deepens the understanding of chirality transfer and amplification across different hierarchical levels.

Substituent effects on Axial Chiral Compound Enantiomers: Synthesis and Crystal Structures of Axially Chiral 1,3,4-Oxadiazole Thioethers (Sulfones) based on 2,2′-Bipyridine

The title compounds have been synthesized from 2,2′bipyridine-3,3′-dicarboxylic acid by a multi-step reaction. These compounds were characterized by 1H and 13C NMR spectroscopy and MS, and The molecular structures of their main compounds(5a-j;6a-e) were determined by single crystal X-ray diffraction. The crystal structure shows that the corresponding product also has axial chirality due to the axial chirality of the 2,2′-bipyridine-3,3′-dicarboxylic acid. Moreover, the type and number of axial chirality of these products varies with the substituents, and shows a certain regularity. This paper presents our preliminarily findings on such axially chiral compounds.

Odd viscous flow past a sphere at low but non-zero Reynolds numbers

The measurement of lift on symmetrically shaped obstacles immersed in low Reynolds number flow is the quintessential way to signal odd viscosity. For flow past cylinders, such a lift force does not arise if incompressibility and no-slip boundary conditions are fulfilled, whereas for spheres, a lift force has been found in Stokes flow, which is valid for cases where the Reynolds numbers are negligible and convection can be ignored. When considering the role of convection at low but non-zero Reynolds numbers, two hurdles arise, the Whitehead paradox and the breaking of axial symmetry, which are overcome by the method of matched asymptotic expansions and the Lorentz reciprocal theorem, respectively. We also consider the case where axial symmetry is preserved because the translation of the sphere is aligned with the axis of chirality of odd viscosity. We find that while lift vanishes, the interplay between odd viscosity and convection gives rise to a stream-induced torque.

Asymmetric construction of axial and planar chirality with N-heterocyclic carbene (NHC) organocatalysis

Asymmetric construction of axial and planar chirality with N-heterocyclic carbene (NHC) organocatalysis

Enantioselective Synthesis of Axially Chiral Silacyclohexylidene Oxime Ethers by Chiral Phosphoric Acid Catalysis

The first asymmetric condensation of prochiral silacyclohexanones with hydroxylamines is developed by chiral phosphoric acid catalysis, which provided a facile and straightforward protocol for the enantioselective construction of valuable axially chiral silacyclohexylidene oxime ethers that are otherwise inaccessible. Notably, this constitutes a rare example for accessing silacycles featuring an axial chirality.

Rational Design and Stereodivergent Construction of Enantioenriched Tetrahydro-β-Carbolines Containing Multistereogenic Centers.

Chiral tetrahydro-β-carbolines, as one of the most intriguing subtypes of indole alkaloids, have emerged as the privileged units in plenty of natural products and biologically active molecules with an impressive range of bioactive properties. However, the stereodivergent construction of these valuable skeletons containing multistereogenic centers from readily available starting materials remains very challenging, especially, in view of the introduction of an axial chirality. Herein, we developed an efficient method toward enantioenriched tetrahydro-β-carbolines with readily available tryptophan-derived aldimine esters and allylic carbonates under mild reaction conditions. The reaction proceeds in a sequential fashion involving synergistic Cu/Ir-catalyzed stereodivergent allylation and the Brønsted acid-promoted stereospecific Pictet-Spengler reaction, affording a wide range of chiral tetrahydro-β-carbolines bearing up to four stereogenic centers in good yields with excellent stereoselectivity control. When N-aryl-substituted tryptophan-derived aldimine esters were utilized, notably, a unique C-N heterobiaryl axis could be simultaneously constructed with the formation of the third point stereogenic center in the last cyclization step through dynamic kinetic resolution (DKR). Computational mechanistic studies established a plausible synergistic mechanism for dual Cu/Ir-catalyzed asymmetric allylation and the succeeding protonation-assisted Pictet-Spengler cyclization to complete the annulation. Structure-activity relationship analyses unveil the origins of stereochemistry for the building of one axis and three point stereogenic centers.

N-Heterocyclic Carbene Enabled Copper Catalyzed Asymmetric Synthesis of Pyrimidinyl Phosphine with both Axial and P-Stereogenicity.

P-stereogenic phosphines, renowned for their utility as ligands and catalysts, have been instrumental in the field of asymmetric catalysis. However, the catalytic asymmetric synthesis of chiral ligands possessing both axial and phosphine chirality remains a significant challenge. Here, we present the successful demonstration of a Cu-catalyzed asymmetric C-P construction using in situ generated secondary phosphine and heteroaryl chloride. By introducing a chiral NHC ligand and an achiral diphosphine auxiliary ligand, we effectively alleviated the poisoning effect caused by phosphine(III) compounds and suppressed the nonenantioselective background reaction. The reaction exhibited excellent enantioselectivity, with up to 96 % ee, and good diastereoselectivity, with up to 14 : 1 dr, when employing less sterically hindered secondary phosphines. This particular substrate poses a significant challenge due to its strong poisoning effect in copper catalysis.

Robust Edge Flows in Swarming Bacterial Colonies

Understanding if and how the chirality of biomolecules is transferred across scales into larger components and active processes remains elusive. For instance, flagellated bacteria swim in helical trajectories but chirality seems absent from the active turbulence dynamics they display in dense suspensions. We address this question by examining multiscale dynamics in colonies. We find active turbulence without manifest chirality in the bulk, but wide, clockwise (viewed from the air side) circulation all along the tortuous centimeter-scale external boundary, while similar but counterclockwise flows follow internal boundaries. We trace the origin of these robust edge flows to an unexpected asymmetry at the individual level that is amplified by local interactions. We rationalize our findings with a model of noisy self-propelled particles immersed in a Stokes fluid that accounts faithfully for our observations. Our modeling and experimental efforts reveal that local nematic alignment and hydrodynamic interactions amplify the weak chiral bias in individual motion, promoting the formation of strong edge flows. The likely topological protection of these flows provides robust transport mechanism over large scales. Such robust boundary phenomena in weakly chiral active fluids may inspire new control strategies for active and biological matter. Published by the American Physical Society 2024

Structure and noncovalent interaction analysis of half-sandwich chiral-at-metal organoruthenium complexes with planar and η6-arene-metal axial chirality

The preparation of organometallic compounds has provided new molecular complexity in molecular science. The stereochemistry of organometallics has long been a great challenge due to the large atom radius and more valency. Herein, eight ruthenium piano-stool shaped Ru complexes 2a-d and 3a-d with η6-planar chirality and Ru-center chirality were successfully synthesized and resolved, and the absolute configurations were determined by X-ray diffraction analysis. Racemization experiment revealed the stability differences of the Ru complexes in various solvents. Furthermore, in asymmetric unit of complex 3b, there are two conformers bearing opposite η6-arene-Ru axial chirality. In the supramolecular organization, all of the Ru complexes are stabilized by hydrogen bonding, C-H···π and Cl/I···π interactions. π···π interaction was only observed in complex 3b. The Hirshfeld surface analysis and 2D fingerprint plot show that the eight complexes have a similar contribution composed of different noncovalent interactions to the stabilization of crystal packing. Interestingly, only complex 3b has 3.5% C···C interaction. The pairwise interaction energies were calculated using CE-B3LYP energy model and further visualized by 3D-energy framework, which show that the dominant interaction for all complexes is dispersion. Theoretical energies of each conformer of complex 2a-d and 3a-d with η6-arene rotated at different angles was calculated by DFT method, and the energy barrier between the two conformations was around 2-3 kcal/mol. Halide ligand exchange experiments on complex (SRu)-1a were performed and the plausible mechanism was proposed. These results have provided new evidence for the design of molecules with specific fine stereochemical information for potential applications in medicinal and material chemistry.

Divergent asymmetric reactions of α-alkenyl ketones with β,γ-alkynyl-α-imino esters enabled by chiral phosphoric acids

Divergent asymmetric synthesis provides access to a wide range of isomers from the same starting material by modifying the reaction conditions, which plays an important role in the efficient construction of a structurally diverse molecular library for structure-activity relationship studies. In this work, we present the divergent asymmetric addition of α-alkenyl ketones with β,γ-alkynyl-α-imino esters enabled by chiral phosphoric acid catalysis. Despite the challenging presence of multiple reactive sites in both components, we successfully achieved the regioselective synthesis of both α-1,2-addition α-tertiary amines and γ-1,4-addition allenes with good to high regio-, diastereo- and enantioselectivities by modifying the reaction conditions. Moreover, the stereodivergent asymmetric synthesis of the four allene stereoisomers bearing contiguous central and axial chirality was achieved by adjusting the E/Z configuration of the α-alkenyl ketone substrates.