Article
|
Open Access
Featured
-
-
Article
| Open AccessEnantioselective copper-catalyzed azidation/click cascade reaction for access to chiral 1,2,3-triazoles
Catalytic asymmetric click reactions of azides and alkynes for chiral triazole synthesis remains a challenge, due to the limited catalytic systems and substrate scope. Herein, the authors report the enantioselective azidation/click cascade reaction of N-propargyl-β-ketoamides via copper catalysis, affording a variety of chiral 1,2,3-triazoles.
- Ling-Feng Jiang
- , Shao-Hua Wu
- & Qing-Hai Deng
-
Article
| Open AccessThymoquinone as an electron transfer mediator to convert Type II photosensitizers to Type I photosensitizers
Developing Type I photosensitizers (PSs) is vital for tackling hypoxic intolerance of photodynamic therapy in the hypoxic microenvironment, but elusive due to the lack of a general molecular design strategy. Here the authors report a universal and simple method to covert traditional Type II PSs to Type I PSs.
- Jiahao Zhuang
- , Guobin Qi
- & Bin Liu
-
Article
| Open AccessChiral dinitrogen ligand enabled asymmetric Pd/norbornene cooperative catalysis toward the assembly of C–N axially chiral scaffolds
The preparation of C − N axially chiral compounds, a class of privileged scaffolds in pharmaceuticals, advanced materials and organic synthesis, has recently attracted significant interest. Herein the authors report a chiral dinitrogen ligand promoted asymmetric Catellani reaction for the synthesis of C–N axially chiral scaffolds.
- Liang Jin
- , Ya Li
- & Bing-Feng Shi
-
Article
| Open AccessEnantioselective synthesis of chiral amides by carbene insertion into amide N–H bond
Chiral amides are important structure in many natural products and pharmaceuticals, yet their efficient synthesis from simple amide feedstock remains challenge due to its weak Lewis basicity. Here, the authors report the enantioselective synthesis of chiral amides by N-alkylation of primary amides via Rh-catalyzed carbene N–H insertion reaction.
- Xuan-Ge Zhang
- , Zhi-Chun Yang
- & Qi-Lin Zhou
-
Article
| Open AccessDifluorocarbene-induced [1,2]- and [2,3]-Stevens rearrangement of tertiary amines
The Stevens rearrangements are a fundamental and powerful tool in the synthetic organic chemistry repertoire, but these transformations are known to be limited in their tolerance for some common functional groups. Here, the authors present a methodology that uses a difluorocarbene unit to induce a Stevens rearrangement, which enables smooth inclusion of allylic and propargyl moieties in the transformation.
- Jianke Su
- , Yu Guo
- & Qiuling Song
-
Article
| Open AccessHeterogeneous organophotocatalytic HBr oxidation coupled with oxygen reduction for boosting bromination of arenes
Developing mild photocatalytic bromination strategies using sustainable bromo source has been attracting intense interests, but there is still much room for improvement. Here, the authors report heterogenous organophotocatalytic HBr oxidation coupled with oxygen reduction to furnish Br2 and H2O2 for effective bromination of arenes.
- Jie Wang
- , Jiahao Liang
- & Bin Liu
-
Article
| Open AccessA combined experimental and computational study of ligand-controlled Chan-Lam coupling of sulfenamides
Sulfenamides are a class of divalent sulfur-derived scaffolds featuring an S-N bond with many industrial applications, however, they are also challenging substrates for synthetic transformations. Here, the authors present a highly chemoselective ligand-controlled Chan–Lam coupling of sulfenamides as a straightforward route to N-arylated sulfenamides.
- Kaiming Han
- , Hong Liu
- & Tiezheng Jia
-
Article
| Open AccessBicarbonate-binding catalysis for the enantioselective desymmetrization of keto sulfonium salts
Although anion-binding processes are well-known for their crucial role in molecular recognition, this type of phenomenon has only recently been utilized for catalysis. Here, the authors present an enantioselective desymmetrization of cyclic keto sulfonium salts through enantioselective deprotonation/ring opening process by anion-binding catalysis.
- José Alemán
- , Jorge Humbrías-Martín
- & Jose A. Fernández-Salas
-
Article
| Open AccessWhy •CF2H is nucleophilic but •CF3 is electrophilic in reactions with heterocycles
Empirically observed regiochemistries indicate that the CF2H radical has a nucleophilic character similar to alkyl radicals, but the CF3 radical is electrophilic in reactions with heterocycles. Here, the authors report DFT calculations, reproducing experimental selectivities and leading to an explanation of this difference.
- Meng Duan
- , Qianzhen Shao
- & K. N. Houk
-
Article
| Open AccessAtroposelective synthesis of biaxial bridged eight-membered terphenyls via a Co/SPDO-catalyzed aerobic oxidative coupling/desymmetrization of phenols
Biaryl compounds with an axial chirality are valuable architectures but few methods have been developed for the construction of bridged biaryls, a subclass of these compounds that bear a tether to connect the two arenes and form a medium-sized ring. Here, the authors design a Co/SPDO-catalyzed aerobic oxidative coupling/desymmetrization sequence of prochiral phenols for the enantioselective synthesis of biaxial bridged m-terphenyls embedded in an azocane.
- Shuang-Hu Wang
- , Shi-Qiang Wei
- & Tong-Mei Ding
-
Article
| Open AccessPhoto-cycloaddition reactions of vinyldiazo compounds
Heterocycles, highly prized by the pharmaceutical industry, are often constructed from diazo compounds. Here, the authors report that direct photolysis of vinyldiazo compounds followed by [3+2]-cycloaddition gives access to these motifs.
- Ming Bao
- , Klaudia Łuczak
- & Michael P. Doyle
-
Article
| Open AccessCatalytic asymmetric synthesis of planar-chiral dianthranilides via (Dynamic) kinetic resolution
Chirality has long fascinated chemists, but asymmetric synthesis has largely focused on central, axial, and helical chirality to date. Here, the authors synthesize dianthranilides with planar chirality, via cinchona alkaloid-catalyzed (dynamic) kinetic resolution.
- Chun-Yan Guan
- , Shuai Zou
- & Guang-Jian Mei
-
Article
| Open AccessCatalytic asymmetric [4 + 2] dearomative photocycloadditions of anthracene and its derivatives with alkenylazaarenes
While significant progress has been made in classical Diels-Alder reactions, the use of simple and inert feedstock chemicals under mild reaction conditions still remains challenging. Here the authors present the development of catalytic asymmetric [4 + 2] dearomative photocycloaddition involving anthracene and its derivatives with alkenylazaarenes.
- Dong Tian
- , Wenshuo Shi
- & Zhiyong Jiang
-
Article
| Open AccessCobalt-catalyzed cross-electrophile coupling of alkynyl sulfides with unactivated chlorosilanes
Transition-metal catalyzed cross-electrophile coupling (XEC) is a powerful tool for the construction of molecules but XEC between carbon electrophile and chlorosilanes to access organosilicon compounds remains underdeveloped. Here the authors disclose a highly efficient cobalt-catalyzed cross-electrophile alkynylation of a broad range of unactivated chlorosilanes with alkynyl sulfides as a stable and practical alkynyl electrophiles.
- Donghui Xing
- , Jinlin Liu
- & Liangbin Huang
-
Article
| Open AccessEnantioselective nickel-catalyzed anodic oxidative dienylation and allylation reactions
Precision control of stereochemistry in radical reactions remains a formidable challenge. Here the authors demonstrate an electricity driven asymmetric Lewis acid catalysis to facilitate asymmetric dienylation and allylation reactions, resulting in the formation of all-carbon quaternary stereocenters.
- Qinglin Zhang
- , Jiayin Zhang
- & Chang Guo
-
Article
| Open AccessTitanium catalyzed [2σ + 2π] cycloaddition of bicyclo[1.1.0]-butanes with 1,3-dienes for efficient synthesis of stilbene bioisosteres
Natural stilbenes show significant potential in the prevention and treatment of diseases due to their diverse pharmacological activities. Here the authors present a mild and effective Ti-catalyzed intermolecular radical-relay cycloaddition reaction with good regio- and trans-selectivity offering rapid access to structurally diverse stilbene bioisosteres.
- Yonghong Liu
- , Zhixian Wu
- & Lei Shi
-
Article
| Open AccessOrganocatalytic skeletal reorganization for enantioselective synthesis of S-stereogenic sulfinamides
The enantioselective synthesis of S-stereogenic sulfinamides has garnered considerable attention due to their unique structural and physicochemical properties but catalytic asymmetric synthesis of sulfinamides still remains challenging. Here, the authors present the synthesis of S-stereogenic sulfinamides through the peptide-mimic phosphonium salt-catalyzed asymmetric skeletal reorganization of simple prochiral and racemic sulfoximines.
- Zanjiao Liu
- , Siqiang Fang
- & Tianli Wang
-
Article
| Open AccessDiastereoselective dearomatization of indoles via photocatalytic hydroboration on hydramine-functionalized carbon nitride
Dearomative hydroboration of predominantly existing indole derivatives provides a straightforward strategy to synthesize boryl indolines, but developing eco-friendly methods for remains challenging. Here, the authors develop a method for heterogeneous photocatalytic trans-hydroboration of indole derivatives with NHC-borane.
- Qiao Zhang
- , Wengang Xu
- & Mingbo Wu
-
Article
| Open AccessObservation of unusual outer-sphere mechanism using simple alkenes as nucleophiles in allylation chemistry
Allylic substitution reaction of alkenes has been well-developed, but it has limitations, partly due to the intrinsic predilection for an inner-sphere mechanism. Herein, the authors present an outer-sphere mechanism in Rh-catalyzed allylic substitution reaction of simple alkenes using gem-difluorinated cyclopropanes as allyl surrogates.
- Yaxin Zeng
- , Han Gao
- & Ying Xia
-
Article
| Open AccessA facile synthesis of α,β-unsaturated imines via palladium-catalyzed dehydrogenation
α,β-unsaturated compounds serve as versatile synthons in organic chemistry, but the α,β-desaturation of aliphatic imines is challenging due to easy hydrolysis and preferential dimerization. Herein, the authors report the synthesis of α,β-unsaturated imines by employing a pre-fluorination and palladium-catalyzed dehydrogenation reaction sequence.
- Chunyang Zhao
- , Rongwan Gao
- & Junkai Fu
-
Article
| Open AccessPara-selective nitrobenzene amination lead by C(sp2)-H/N-H oxidative cross-coupling through aminyl radical
Direct radical C–H amination strategies have exhibited innovation, but challenges remain with C–H amination of electron-poor nitroarenes due to the essence of the electron-deficient nitrogen radical. Herein, the authors report a transition metal-free dehydrogenative C(sp2)-H/N-H cross-coupling between electron-poor nitroarenes and amines.
- Zhen Zhang
- , Shusheng Yue
- & Hu Cai
-
Article
| Open AccessLate-stage benzenoid-to-troponoid skeletal modification of the cephalotanes exemplified by the total synthesis of harringtonolide
Many natural products exist as families of structurally similar molecules, and therefore developing skeletal modifications of common intermediates offers flexible and powerful approaches for target synthesis. Here, the authors report a single-atom insertion into the framework of the benzenoid subfamily, providing access to the troponoid congeners.
- Stefan Wiesler
- , Goh Sennari
- & Richmond Sarpong
-
Article
| Open AccessIntroduction of the difluoromethyl group at the meta- or para-position of pyridines through regioselectivity switch
The direct C−H-difluoromethylation of pyridines represents a highly efficient economic way to access azines. However, the direct meta-difluoromethylation of pyridines remains elusive. Here, the authors demonstrate switchable meta- as well as para-C−H difluoromethylation of pyridines through radical processes by using oxazino pyridine intermediates.
- Pengwei Xu
- , Zhe Wang
- & Armido Studer
-
Article
| Open AccessAsymmetric C–H Dehydrogenative Alkenylation via a Photo-induced Chiral α‑Imino Radical Intermediate
The direct alkenylation with simple alkenes stands out as the most ideal yet challenging strategy for obtaining high-valued desaturated alkanes. Herein, the authors present a direct asymmetric dehydrogenative α-C(sp3)-H alkenylation of carbonyls based on synergistic photoredox-cobalt-chiral primary amine catalysis under visible light.
- Zongbin Jia
- , Liang Cheng
- & Sanzhong Luo
-
Article
| Open AccessRapid and scalable photocatalytic C(sp2)–C(sp3) Suzuki−Miyaura cross-coupling of aryl bromides with alkyl boranes
In recent years a growing demand for drug design approaches that incorporate a higher number of sp3-hybridized carbons fuelled the development of innovative cross-coupling strategies to reliably introduce aliphatic fragments. Here, the authors present a powerful approach for the light-mediated B-alkyl Suzuki−Miyaura crosscoupling between alkyl boranes and aryl bromides.
- Ting Wan
- , Luca Capaldo
- & Timothy Noël
-
Article
| Open AccessDeciphering complexity in Pd–catalyzed cross-couplings
Knowledge about the full reaction signature, such as the complete profile of products and side-products is important in accelerating discovery chemistry. Here, the authors report a methodology using high-throughput experimentation and multivariate data analysis to examine Palladium- catalyzed cross-coulpling reactions.
- George E. Clarke
- , James D. Firth
- & Ian J. S. Fairlamb
-
Article
| Open AccessN2 cleavage by silylene and formation of H2Si(μ-N)2SiH2
So far, only homoleptic N2 complexes of silicon have been reported under matrix-isolation conditions including but the activation of more inert nitrogen by silylenes remains challenging. Here the authors report on the activation of dinitrogen by silylenes under cryogenic conditions.
- Liyan Cai
- , Bing Xu
- & Xuefeng Wang
-
Article
| Open Access“On-Water” accelerated dearomative cycloaddition via aquaphotocatalysis
Developing water compatible synthetic methods for Sulfur(VI) fluoride exchange (SuFEx) chemistry is of paramount importance. Here the authors demonstrate a catalytic dearomative [2+2] photocycloaddition that significantly speeds up the synthesis of heterocyclic alkyl SuFEx hubs, leveraging the unique reactivity at the water-oil interface.
- Soo Bok Kim
- , Dong Hyeon Kim
- & Han Yong Bae
-
Article
| Open AccessOne pot conversion of phenols and anilines to aldehydes and ketones exploiting α gem boryl carbanions
For the carbonylation reactions to synthesize aldehyde, ester, amide, and other carbonyl derivatives, a transition metal-free and CO- free reaction was challenging but highly demanded. Here, the authors report a transition metal-free and CO- free method for deoxygenetive/denitrogenetive conversion of phenols and anilines to aldehydes and ketones.
- Kanak Kanti Das
- , Debasis Aich
- & Santanu Panda
-
Article
| Open AccessElectrochemical C−H deuteration of pyridine derivatives with D2O
Despite the established C − H deuteration of pyridine derivatives synthetic methods with good D-incorporation, under milder conditions with easy operation procedures is still on the way. Here, the authors develop a straightforward, metal-free, and acid-/base-free electrochemical C4-selective C − H deuteration of pyridine derivatives with high selectivity and excellent D-incorporation at room temperature, which use D2O as economic and convenient D-source.
- Zhiwei Zhao
- , Ranran Zhang
- & Youai Qiu
-
Article
| Open AccessDecarboxylative stereoretentive C–N coupling by harnessing aminating reagent
Accessing chiral alkylamines is highly important due to their ubiquity in bioactive molecules. Here, the authors present the development of stereoretentive decarboxylative amidation of carboxylic acids using dioxazolone under ambient conditions.
- Jeonguk Kweon
- , Bumsu Park
- & Sukbok Chang
-
Article
| Open AccessEnantioselective synthesis of chiral α,α-dialkyl indoles and related azoles by cobalt-catalyzed hydroalkylation and regioselectivity switch
Catalytic and enantioselective construction of chiral α,α-dialkyl indoles represents an important yet challenging objective to be developed. Herein the authors describe a cobalt catalyzed enantioselective anti-Markovnikov alkene hydroalkylation via the remote stereocontrol for the synthesis of α,α-dialkyl indoles and other N-heterocycles.
- Jiangtao Ren
- , Zheng Sun
- & Zhihui Shao
-
Article
| Open AccessCarbon–nitrogen transmutation in polycyclic arenol skeletons to access N-heteroarenes
Developing skeletal editing tools, especially to realize the single-atom transmutation in a ring system without altering the ring size is challenging. Here, the authors introduce a skeletal editing strategy that enables polycyclic arenols to be readily converted into N-heteroarenes through carbon–nitrogen transmutation.
- Hong Lu
- , Yu Zhang
- & Hao Wei
-
Article
| Open AccessStereospecific syn-dihalogenations and regiodivergent syn-interhalogenation of alkenes via vicinal double electrophilic activation strategy
Restricted reaction mechanism of anti-dihalogenation of alkenes makes it challenging to alter the diastereochemical course into the complementary syn-dihalogenation process. Here, the authors report a conceptually distinctive strategy for the simultaneous double electrophilic activation of the two alkene carbons from the same side to realize syn-dihalogenation.
- Hyeon Moon
- , Jungi Jung
- & Won-jin Chung
-
Article
| Open AccessDinuclear gold-catalyzed divergent dechlorinative radical borylation of gem-dichloroalkanes
The widespread use of organoboronic acids has prompted the development of synthetic methodologies to meet the demands on structural diversity and functional group tolerance. Herein, the authors disclose a divergent radical dechloroborylation reaction enabled by dinuclear gold catalysis with visible light irradiation.
- Cheng-Long Ji
- , Hongliang Chen
- & Jin Xie
-
Article
| Open AccessDiastereo-divergent synthesis of chiral hindered ethers via a synergistic calcium(II)/gold(I) catalyzed cascade hydration/1,4-addition reaction
Developing an efficient method for the stereocontrolled synthesis of all stereoisomers of chiral hindered ethers is highly desirable but challenging. Here, the authors report an asymmetric cascade reaction catalyzed by a bimetallic catalytic system with control over the configuration of the stereocenters of tetra-aryl substituted ethers.
- Xiangfeng Lin
- , Xia Mu
- & Can Li
-
Article
| Open AccessSwitchable chemoselective aryne reactions between nucleophiles and pericyclic reaction partners using either 3-methoxybenzyne or 3-silylbenzyne
Due to the electrophilic nature of arynes, it is very challenging to control chemoselectivity, when substrates possess multiple competing reaction sites. Here, the authors demonstrate that chemoselective control between two major types of benzyne transformation is accomplished by varying the 3-substituent on aryne intermediate.
- Hongcheng Tan
- , Shuxin Yu
- & Yang Li
-
Article
| Open AccessCatalytic 1,1-diazidation of alkenes
Compared to well-developed catalytic 1,2-diazidation of alkenes, the corresponding catalytic 1,1-diazidation of alkenes has not been realized. Here, the authors report an efficient approach for catalytic 1,1-diazidation of alkenes by redox-active selenium catalysis.
- Wangzhen Qiu
- , Lihao Liao
- & Xiaodan Zhao
-
Article
| Open AccessPathway-divergent coupling of 1,3-enynes with acrylates through cascade cobalt catalysis
The development of divergent reaction pathways controlled by different ligands is a critical goal. Here the authors describe a cobalt-catalyzed strategy for cascade coupling of 1,3-enynes with two molecules of acrylates through three reaction modes.
- Heng Wang
- , Xiaofeng Jie
- & Fanke Meng
-
Article
| Open AccessDehydroxylative radical N-glycosylation of heterocycles with 1-hydroxycarbohydrates enabled by copper metallaphotoredox catalysis
N-Glycosylated heterocycles play important roles in biological systems and drug development, but the synthesis heavily relies on ionic N-glycosylation. Herein, the authors report a dehydroxylative radical method for synthesizing N-glycosides by leveraging copper metallaphotoredox catalysis.
- Da-Peng Liu
- , Xiao-Sen Zhang
- & Xiang-Guo Hu
-
Article
| Open AccessPolarizability matters in enantio-selection
Polarizability, a property that is closely related to softness in the classic theory of Hard and Soft Acids and Bases (HSAB), has been largely overlooked in connecting with enantio-selection in the past. Here, the authors show local polarizability-based electronic effects can rationalize a wide range of stereochemical outcomes in widely-known asymmetric catalytic reactions.
- Fumin Chen
- , Yu Chen
- & Xiangyou Xing
-
Article
| Open AccessIterative SuFEx approach for sequence-regulated oligosulfates and its extension to periodic copolymers
The synthesis of sequence-regulated oligosulfates has not yet been established due to the difficulties in precise reactivity control. Here, the authors report a multi-directional divergent iterative method to furnish oligosulfates based on a chain homologation approach, in which the fluorosulfate unit is regenerated.
- Min Pyeong Kim
- , Swatilekha Kayal
- & Sung You Hong
-
Article
| Open AccessPalladium-catalyzed asymmetric carbene coupling en route to inherently chiral heptagon-containing polyarenes
Developing facile and direct synthesis routes for enantioselective construction of cyclic π-conjugated molecules is crucial but the chirality orginiating from the distorted structure around heptagon-containing polyarenes is largely overlooked. Herein the authors present a highly enantioselective synthesis for fabrication of all carbon heptagon-containing polyarenes via palladium-catalyzed carbene-based cross–coupling of benzyl bromides and N-arylsulfonylhydrazones.
- Huan Zhang
- , Chuan-Jun Lu
- & Ren-Rong Liu
-
Article
| Open AccessNoncovalent interaction with a spirobipyridine ligand enables efficient iridium-catalyzed C–H activation
Exploitation of noncovalent interactions has received much attention for the design of metal catalysts. However, because of the weak nature, CH-π interactions have been less utilized for the control of organic reactions. Here, the authors report that the CH-π interaction can be used to kinetically accelerate catalytic C-H activation of arenes.
- Yushu Jin
- , Boobalan Ramadoss
- & Laurean Ilies
-
Article
| Open AccessSelenium catalysis enables negative feedback organic oscillators
Multiple autocatalytic reactions producing thiols are known, but negative feedback loop motifs are unavailable for thiol chemistry. Here, the authors develop a negative feedback loop based on the selenocarbonates, in which thiols induce the release of aromatic selenols that catalyze the oxidation of thiols by organic peroxides.
- Xiuxiu Li
- , Polina Fomitskaya
- & Sergey N. Semenov
-
Article
| Open AccessPhotocatalytic Z/E isomerization unlocking the stereodivergent construction of axially chiral alkene frameworks
The stereospecific Z/E isomerization of tetrasubstituted alkenes remains underdeveloped, thus lacking in a stereodivergent synthesis of axially chiral alkenes. Here, authors report the atroposelective synthesis of tetrasubstituted alkene analogues by asymmetric allylic substitution-isomerization, followed by the photocatalyzed Z/E isomerization.
- Jie Wang
- , Jun Gu
- & Ying He
-
Article
| Open AccessOrganocatalytic desymmetrization provides access to planar chiral [2.2]paracyclophanes
Planar chiral [2.2]paracyclophanes have a wide range of applications in asymmetric synthesis and materials science. However, they are accessed via time-consuming chiral separations or kinetic resolution approaches. Here, the authors report a simple, metal-free protocol for organocatalytic desymmetrization of prochiral diformyl[2.2]paracyclophanes.
- Vojtěch Dočekal
- , Filip Koucký
- & Jan Veselý
-
Article
| Open AccessNickel-catalyzed switchable arylative/endo-cyclization of 1,6-enynes
Divergent functionalizations of pi bonds allow for synthetic chemists to move from simplicity to complexity. Here, the authors report a nickel-catalyzed switchable arylation/cyclization of 1,6-enynes in which the nature of the ligand dictates the regioselectivity of alkyne arylation, while the electrophilic trapping reagents determine the selectivity of the cyclization mode.
- Wenfeng Liu
- , Wei Li
- & Wangqing Kong
-
Article
| Open AccessPaired electrocatalysis unlocks cross-dehydrogenative coupling of C(sp3)-H bonds using a pentacoordinated cobalt-salen catalyst
Cross-dehydrogenative coupling (CDC) of C-H bonds is an ideal approach for C-C bond construction but suffers from low selectivity of similar C-H bonds. Here, the authors describe a highly selective paired electrocatalysis strategy towards CDC combining hydrogen evolution reaction catalysis with hydride transfer catalysis.
- Ke Liu
- , Mengna Lei
- & Sheng Zhang