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Axially chiral diaryl ethers are a type of unique atropisomers bearing two potential axes, which have potential applications in a variety of research fields. However, the catalytic enantioselective synthesis of these diaryl ether atropisomers is largely underexplored when compared to the catalytic asymmetric synthesis of biaryl or other types of atropisomers. Herein, we report a highly efficient catalytic asymmetric synthesis of diaryl ether atropisomers through an organocatalyzed enantioselective desymmetrization protocol. The chiral phosphoric acid‐catalyzed asymmetric electrophilic aromatic aminations of the symmetrical 1,3‐benzenediamine type substrates afforded a series of diaryl ether atropisomers in excellent yields and enantioselectivities. The facile construction of heterocycles by the utilizations of the 1,2‐benzenediamine moiety in the products provided access to a variety of structurally diverse and novel azaarene‐containing diaryl ether atropisomers. [ABSTRACT FROM AUTHOR]

Axially chiral diaryl ethers are a type of unique atropisomers bearing two potential axes, which have potential applications in a variety of research fields. However, the catalytic enantioselective synthesis of these diaryl ether atropisomers is largely underexplored when compared to the catalytic asymmetric synthesis of biaryl or other types of atropisomers. Herein, we report a highly efficient catalytic asymmetric synthesis of diaryl ether atropisomers through an organocatalyzed enantioselective desymmetrization protocol. The chiral phosphoric acid‐catalyzed asymmetric electrophilic aromatic aminations of the symmetrical 1,3‐benzenediamine type substrates afforded a series of diaryl ether atropisomers in excellent yields and enantioselectivities. The facile construction of heterocycles by the utilizations of the 1,2‐benzenediamine moiety in the products provided access to a variety of structurally diverse and novel azaarene‐containing diaryl ether atropisomers. [ABSTRACT FROM AUTHOR]

The first kinetic resolution of hydroquinoline derivatives with α,α‐disubstitution has been achieved through asymmetric remote aminations with azodicarboxylates enabled by chiral phosphoric acid catalysis. Mechanistic studies suggest a monomeric catalyst pathway proceeding through rate‐ and enantio‐determining electrophilic attack promoted by a network of attractive non‐covalent interactions between the substrate and catalyst. Facile subsequent removal and transformations of the newly introduced hydrazine moiety enable these protocols to serve as powerful tools for asymmetric synthesis of N‐heterocycles with α,α‐disubstitution. [ABSTRACT FROM AUTHOR]

The first kinetic resolution of hydroquinoline derivatives with α,α‐disubstitution has been achieved through asymmetric remote aminations with azodicarboxylates enabled by chiral phosphoric acid catalysis. Mechanistic studies suggest a monomeric catalyst pathway proceeding through rate‐ and enantio‐determining electrophilic attack promoted by a network of attractive non‐covalent interactions between the substrate and catalyst. Facile subsequent removal and transformations of the newly introduced hydrazine moiety enable these protocols to serve as powerful tools for asymmetric synthesis of N‐heterocycles with α,α‐disubstitution. [ABSTRACT FROM AUTHOR]

In this short review, we summarize the recent developments on thermo-driven C(sp3)–O bond radical scission methods and their applications in the construction of C(sp3)–C bonds via conjugate addition with activated double bonds and reductive coupling mediated by economic 3d metals, in particular nickel. We have arranged the review based on three approaches for C(sp3)–O bond radical scission (vide infra). After generating the radical intermediates, their subsequent transformation into C(sp3)–C bonds enabled by C(sp3)–O cross-electrophile coupling with carbon electrophiles is discussed in detail. 1 Introduction 2 Direct Single-Electron Transfer to a C(sp3)–O Bond 3 Radical Scission of Activated C(sp3)–O Bonds via Single-Electron Transfer to Protecting Groups 4 In Situ Activation of Alcohols 5 Summary and Outlook [ABSTRACT FROM AUTHOR]

Herein, the use of economically and environmentally friendly bis(pinacolato)diboron (B2Pin2) is described as a non‐metallic reductant in mediating Ni‐catalyzed C(sp3)–C(sp2) reductive cross‐coupling of alkyl electrophiles with aryl/vinyl halides. This method exhibits excellent suitability for heteroaryl halides and alkyl halides/Katritzky salts. The present study is compatible with an in situ halogenation of alcohol method, allowing for selective mono‐functionalization of diols and bio‐relevant alcohols (e.g., carbohydrates). The use of B2Pin2 shows potential for easy scalability without introducing additional metal impurities into the products. It is observed for the first time in the realm of cross‐electrophile coupling chemistry that B2Pin2 can sever as a reductant to reduce NiII to Ni0. This mechanistic insight may inspire the development of new reductive bond‐forming methodologies that can otherwise be difficult to achieve with a metal reductant. [ABSTRACT FROM AUTHOR]

An efficient approach for asymmetric synthesis of planar‐chiral macrocycles (paracyclophanes) has been disclosed through enantioselective electrophilic aromatic aminations with azodicarboxylates enabled by chiral phosphoric acid catalysis. A wide range of chiral macrocycles bearing varied ring sizes (16 to 23‐membered) and functional group‐containing ansa chains were readily afforded using this method, with excellent yields and high enantioselectivities (23 examples, up to 99.5 : 0.5 er). Experimental studies and DFT calculations were performed to elucidate the mechanism and origin of stereoselectivities of these reactions. Preliminary utilization of the planar‐chiral macrocycle as chiral organocatalyst showcased the potential applications of these novel chiral skeletons. [ABSTRACT FROM AUTHOR]

An efficient approach for asymmetric synthesis of planar‐chiral macrocycles (paracyclophanes) has been disclosed through enantioselective electrophilic aromatic aminations with azodicarboxylates enabled by chiral phosphoric acid catalysis. A wide range of chiral macrocycles bearing varied ring sizes (16 to 23‐membered) and functional group‐containing ansa chains were readily afforded using this method, with excellent yields and high enantioselectivities (23 examples, up to 99.5 : 0.5 er). Experimental studies and DFT calculations were performed to elucidate the mechanism and origin of stereoselectivities of these reactions. Preliminary utilization of the planar‐chiral macrocycle as chiral organocatalyst showcased the potential applications of these novel chiral skeletons. [ABSTRACT FROM AUTHOR]

Asymmetric functionalizations of α‐sulfanyl cyclic ketones were realized via chiral phosphoric acid catalyzed enantioselective addition reactions with aldimines, azodicarboxylates and allenamides. A series of chiral organosulfur compounds possessing sulfur‐containing tetrasubstituted stereocenters were accessed via these methods, with excellent regioselectivities and high stereoselectivities. [ABSTRACT FROM AUTHOR]

[Display omitted] Methods of copper-catalyzed alkylation of indoles and anilines with tertiary alkyl bromides were reported. These protocols provided various N - tert -alkyl 3-substituted indoles and electron-deficient N - tert -alkyl anilines in moderate to good yields via C N coupling. [ABSTRACT FROM AUTHOR]

An AgI-mediated ethoxycarbonyldifluoromethylation of isocyanides has been developed. This radical cascade reaction involves the addition of difluoromethylene radical to the isocyanide functionality, and subsequent homolytic aromatic substitution to give difluoromethylated phenanthridines with a good functional-group tolerance. [ABSTRACT FROM AUTHOR]

A simple AgI-mediated direct difluoromethylation reaction of activated alkenes by using TMSCF2COOEt (TMS = trimethylsilyl) under mild reaction conditions has been described. This reaction tolerates a variety of functional groups and allows for a highly efficient synthesis of various difluoro-containing oxindoles. Mechanistic investigations indicate that a difluoromethyl radical initiated the cascade sequence by undergoing an addition reaction to the alkene. [ABSTRACT FROM AUTHOR]

An efficient silver‐promoted decarboxylative gem‐difluoromethylenation of aryl‐ or alkyl‐substituted α,β‐unsaturated carboxylic acids with readily available benzo‐1,3‐diazolic difluoromethyl bromides has been developed. This convenient transformation demonstrated good functional‐group tolerability and broad substrate scope, and afforded the allylic difluorides in good to excellent yields with exclusive E‐stereoselectivity under mild reaction conditions. [ABSTRACT FROM AUTHOR]

Simple Summary: Forage oat is an important feed resource in the world. Few studies on the application of different bacterial additives in forage oat silage have been found, which limits the utilization and promotion of oat silage in animal husbandry. In this study, we compared the fermentation quality and in vitro gas production of oat silage treated with four additives (Lactiplantibacillusplantarum F1,LP; Lacticaseibacillusrhamnosus XJJ01, LR; Lacticaseibacillusparacasei XJJ02, LC; and Propionibacterium acidipropionici 1.1161, PP). The results show that compared to the CK group (without additives), the LR group had a higher dry matter content, while the LP group showed an improvement in fermentation quality. At the same time, the bacterial community in the LR group was also different from that in other groups. The treatments of PP and LC had no significant effects on fermentation quality, but the in vitro gas production was significantly reduced in the treated oat silage. These results could help us to optimize the utilization of forage oat silage in balanced ruminant diets. Bacterial inoculants are considered as a good choice for successful ensiling, playing a key role in improving the silage quality. However, the potential of different bacteria, especially the propionic acid bacteria, in forage oat ensiling is yet to be explored. Therefore, the purpose of this study was to investigate the regulation effects of different bacterial additives on the fermentation quality of forage oat silage. Four additives (Lactiplantibacillus plantarum F1, LP; Lacticaseibacillus 0rhamnosus XJJ01, LR; Lacticaseibacillus paracasei XJJ02, LC; and Propionibacterium acidipropionici 1.1161, PP; without additives, CK) were inoculated in forage oat silage, and the fermentation quality and organic compounds were determined after 60 days of ensiling. Notably, LR showed higher dry matter preservation compared to other additives and CK. In addition, LP and LR showed strong lactic acid synthesis capacity, resulting in lower pH compared to other additives and CK. The treatments of PP and LC increased the bacterial diversity in silage, while the bacterial community in the LR group was different from that in other groups. In addition, the PP- and LC-treated oat silage showed significantly lower total in vitro gas production and a lower methane content. These results suggest that LP is more favorable for producing high-quality oat silage than LR, LC, or PP. Both the PP- and LC- treated oat silage may reduce rumen greenhouse gas emissions. [ABSTRACT FROM AUTHOR]

Good's syndrome (GS) is characterized by thymoma combined with adult‐onset immunodeficiency. Diffuse panbronchiolitis (DPB) is a chronic inflammatory airway disease, which predominantly affects East Asians. Japanese scholars have reported extensively about GS combined with DPB or DPB‐like pulmonary manifestation. However, such reports are rare in China. We report here a case of GS in China with DPB as the prominent manifestation and carry out a literature review accordingly. Our review indicates that in adults with DPB‐like clinical manifestations, thymic lesions should be excluded and related immune function tests should be performed to exclude GS to avoid missed diagnosis and misdiagnosis. [ABSTRACT FROM AUTHOR]

An efficient kinetic resolution of N-aryl β-amino alcohols has been developed via asymmetric para-aminations of anilines with azodicarboxylates enabled by chiral phosphoric acid catalysis. Broad substrate scope and high kinetic resolution performances were afforded with this method. Control experiments supported the critical roles of the NH and OH group in these reactions. [ABSTRACT FROM AUTHOR]

A series of cyclohexyl‐fused SPINOL‐derived phosphoric acids (Cy‐SPA) have been developed to catalyze the kinetic resolution of 2‐N‐acylamido tertiary allylic alcohols, providing access to chiral oxazolines bearing C‐2 alkyl substituents with high enantioselectivities (with s‐factors up to 153). Gram‐scale reaction with 1 mol% catalyst loading and transformations of the chiral products demonstrates the value of these methods. [ABSTRACT FROM AUTHOR]

In this new Ag(I)-promoted reaction between N-arylacrylamides and ethyl trimethylsilyldifluoroacetate, the corresponding 3-(2-ethoxycarbonyl-2,2-difluoroethyl)-2-oxo-2,3-dihydro-1H-indoles have been prepared in good yields. [ABSTRACT FROM AUTHOR]

The first AgI-mediated C-H ethoxycarbonyl difluoromethylation with TMSCF2COOEt (TMS = trimethylsilyl) has been developed. The radical difluoromethylation proceeds smoothly to give the difluoromethylated arenes in moderate to high yields with Friedel-Crafts-type regioselectivity. Mechanistic studies indicate that the innate C-H difluoromethylation proceeds through an electrophilic radical-type pathway. [ABSTRACT FROM AUTHOR]

A mild, versatile and efficient method for the silver(i)-catalyzed oxidative decarboxylative gem-difluoromethylenation has been developed. The radical cascade reaction comprises the addition of an oxidatively generated difluoromethylene radical to the isonitrile functionality and subsequent homolytic aromatic substitution. It provides a novel and efficient access to the C–CF2 bond formation. [ABSTRACT FROM AUTHOR]

Efficient direct gem-difluoromethylenation of an sp3-hybridized carbon center in benzyl bromides using benzo-1,3-azolic (oxa-, thia- or aza-) difluoromethyl bromides for construction of a CH2–CF2 linkage has been developed through radical/radical C–C cross-coupling via two separate single electron transfer processes (SET) under the promotion of different copper sources. [ABSTRACT FROM AUTHOR]

The difluoromethylene radical is generated in the title reaction and it reacts with isocyanides to form the C-CF2 bond under mild reaction conditions. [ABSTRACT FROM AUTHOR]

The title reaction between various benzyl bromides and benzo-1,3-oxazolic difluoromethyl bromides tolerates various functional groups and proceeds in generally high yields. [ABSTRACT FROM AUTHOR]