Palladium-Catalyzed Remote Hydrosulfonamidation of Alkenes: Access to Primary N-Alkyl Sulfamides by the SuFEx Reaction
We establish a remote hydrosulfonamidation (HSA) of alkenes using palladium catalysis, where N-fluoro-N-(fluoro-sulfonyl)-carbamate with a sulfur(VI) fluoride moiety is demonstrated as a good amidation reagent. The anti-Markovnikov HSA reaction of terminal alkenes and the remote HSA of internal alkenes are achieved to efficiently yield primary N-alkyl-N-(fluorosulfonyl)-carbamates. In addition, this protocol enables the high-value utilization of alkane by combining the dehydrogenation process. The generated N-alkyl products exhibit a unique reactivity of sulfur(VI) fluorides, which can be directly transferred to N-alkyl sulfamides or amines via the sulfur(VI) fluoride exchange reaction, thereby streamlining their synthesis. Moreover, a (pyridyl) benzazole-type ligand proved to be vital for the excellent chemo- and regioselectivities. This result is published in JACS. Congratulations Chanqi and Zhenye.
Asymmetric 1,n-Remote Aminoacetoxylation of Unactivated Internal Alkenes Enabled by Palladium Catalysis
A palladium-catalyzed asymmetric 1,n-remote aminoacetoxylation of cis-alkenes has been developed using PhI(OAc)2 as an oxidant, providing the acetoxylated lactams with excellent enantioselectivities under mild reaction conditions. The sterically hindered pyridine-oxazoline (Pyox) L3 with a tert-butyl group in oxazoline ring and propyl group in C6 position of pyridinyl is vital for the reaction, where the former is good for asymmetric aminopalladation step and the latter for the chain walking process. The enantioenriched lactam products were proven to be good building blocks for the synthesis of azabicycles.This result is published in Angew. Chem. Congratulations Xintuo.
Site-Selective sp2 C–H Cyanation of Allenes via Copper-Catalyzed Radical Relay
We communicate the site-selective cyanation of the sp2 C–H bond of allenes using the strategy of copper-catalyzed radical relay. The reactions afford various allenyl nitriles directly from simple allenes with a broad substrate scope and a remarkable functional group compatibility under mild conditions. These reactions exhibit excellent site-selectivity toward sp2 C–H, which can be attributed to the unique pocket created by the Cu-bound nitrogen-centered radical. The favorable HAT on sp2 C–H is due to crucial hydrogen bonding between the fluoride bonded to the Cu(II) center and the hydrogen atom at the allylic position. These features enable the late-stage functionalization of druglike bioactive molecules containing an allene motif. This result is published in JACS. Congratulations Zhongming Cheng.
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Copper-Catalyzed Asymmetric Functionalization of Vinyl Radicals for the Access to Vinylarene Atropisomers
A novel asymmetric radical strategy for the straightforward synthesis of atropisomerically chiral vinyl arenes has been established herein, proceeding through copper-catalyzed atroposelective cyanation/azidation of aryl-substituted vinyl radicals. Critical to the success of the radical relay process is the atroposelective capture of the highly reactive vinyl radicals with chiral L*Cu(II) cyanide or azide species. Moreover, these axially chiral vinylarene products can be easily transformed into atropisomerically enriched amides and amines, enantiomerically enriched benzyl nitriles via an axis-to-center chirality transfer process, and an atropisomerically pure organocatalyst for the chemo-, diastereo-, and enantioselective (4 + 2) cyclization reaction. This result is published in JACS. Congratulations Liang Fu & Xin Chen.
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Congratulations
Congratulations to Zhongming Cheng (成忠明) and Wenzheng Fan (樊文峥) on obtaining their PhD degree.
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Regio- and enantioselective remote dioxygenation of internal alkenes
Methods for direct oxygenation of internal alkenes enantioselectively have provided chemists with versatile and powerful toolboxes for the synthesis of optically pure alcohols, which are one of the most privileged structural motifs. Regioselectivity, however, remains a formidable challenge in the functionalization of internal alkenes. Here, we report the palladium-catalyzed highly regio- and enantioselective remote 1,n-dioxygenation (n≥4) of internal alkenes with engineered pyridine-oxazoline (Pyox) ligands. This result is published in Nat. Chem. Congratulations Xiaonan Li.
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Electrophotocatalytic Decoupled Radical Relay Enables Highly Efficient and Enantioselective Benzylic C–H Functionalization
Asymmetric sp3 C–H functionalization has been demonstrated to substantially expedite target molecule synthesis, spanning from feedstocks upgradation to late-stage modification of complex molecules. Herein, we report a highly efficient and sustainable method for enantioselective benzylic C–H cyanation by merging electrophoto- and copper catalysis. A novel catalytic system allows one to independently regulate the hydrogen atom transfer step for benzylic radical formation and speciation of Cu(II)/Cu(I) to effectively capture the transient radical intermediate, through tuning the electronic property of anthraquinone-type photocatalyst and simply modulating the applied current, respectively. This result is published in JACS. Congratulations Wenzheng Fan & Xueyao Zhao.
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Palladium-Catalyzed Remote Hydrooxygenation of Internal Alkenes: An Efficient Access to Primary Alcohols
As a general method for the synthesis of alcohols, the direct oxygenation of alkenes is difficult to afford linear alcohols. Herein, we communicate the remote hydro-oxygenation of alkenes under palladium catalysis, in which both terminal and internal alkenes are suitable to yield the corresponding linear alcohols efficiently. A compatible SelectFluor/silane redox system plays an essential role for the excellent chemo- and regioselectivities. This result is published in JACS. Congratulations Xiang Li.
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Palladium(II)-Catalyzed Enantioselective Hydrooxygenation of Unactivated Terminal Alkenes
A novel Pd(II)-catalyzed enantioselective Markovnikov hydrooxygenation of unactivated terminal alkenes using a substituted pyridinyl oxazoline (Pyox) ligand has been developed. Herein it was discovered that the (EtO)2MeSiH/BQ redox system is vital for the highly selective and efficient hydrooxygenation, where the alkylpalladium(II) species generated from enantioselective oxypalladation step is reduced by silane. This method provides efficient access to optically pure alcohol esters from easily available alkenes with excellent enantioselectivities and features a broad substrate scope. This result is published in J. Am. Chem. Soc.. Congratulations Xintuo Yang.
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Copper-catalyzed radical relay in C(sp3)–H functionalization
Radical-involved transition metal (TM) catalysis has greatly enabled new reactivities in recent decades. Copper-catalyzed radical relay offers enormous potential in C(sp3)–H functionalization which combines the unique regioselectivity of hydrogen atom transfer (HAT) and the versatility of copper-catalyzed cross-coupling. More importantly, significant progress has been achieved in asymmetric C–H functionalization through judicious ligand design. This tutorial review will highlight the recent advances in this rapidly growing area, and we hope this survey will inspire future strategic developments for selective C(sp3)–H functionalization. This result is published in Chemical Society Reviews. Congratulations Zuxiao Zhang.
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Copper-catalysed asymmetric radical cyanation
In this Perspective, we discuss catalytic asymmetric cyanation reactions and the key carbon radicals involved, such as benzylic, allylic and propargylic radicals. In particular, we outline the control of selectivity by considering the mechanism of formation for the carbon radicals as well as the subsequent copper-catalysed radical cyanation step. The carbon radicals can be generated from a diverse range of precursors, which include C–H substrates, alkenes, esters, cyclopropanol and so on. As a consequence, copper-catalysed asymmetric radical cyanation has the potential to expand the scope of catalytic asymmetric cyanation and is expected to find broad utility in organic synthesis and the late-stage functionalization of complex molecules. This Perspective is published in Nature Synthesis. Congratulations Fei Wang
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Catalytic remote hydrohalogenation of internal alkenes
Primary alkyl halides have broad utility as fine chemicals in organic synthesis. The direct halogenation of alkenes is one of the most efficient approaches for the synthesis of these halides. We report the remote oxidative halogenation of alkenes under palladium catalysis via which both terminal and internal alkenes yield primary alkyl halides efficiently. Engineering pyridine-oxazoline ligands by introducing a hydroxyl group is essential for achieving excellent chemo- and regioselectivity. The catalytic system is also good for the mixture of alkene isomers generated from dehydrogenation of alkanes, providing a window to investigate the high-value utilization of inexpensive alkanes. This result is published in Nature Chemistry. Congratulations Xiang Li and Jianbo Jin.
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Enantioselective Copper-Catalyzed Radical Cyanation of Propargylic C–H Bonds: Easy Access to Chiral Allenyl Nitriles
The first enantioselective copper-catalyzed cyanation of propargylic C–H bonds via radical relay was established using novel BoxOTMS ligands, providing an efficient and straightforward tool for the construction of structurally diverse chiral allenyl nitriles in good yields with excellent enantioselectivities. This reaction features high functional group tolerance and mild conditions. In addition, the chiral allene products can be readily converted to other chiral compounds via axis-to-center chirality transfer. This result is published in JACS. Congratulations Ronghua Lu.
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Asymmetric Palladium-Catalyzed Oxycarbonylation of Terminal Alkenes: Efficient Access to β-Hydroxy Alkylcarboxylic Acids
A novel Pd-catalyzed enantioselective oxycarbonylation of alkenes has been established. The ligand with an ethyl group at the C-6 position of Pyox plays a significant role in the intermolecular oxypalladation process, leading to high reactivity and excellent enantioselective control. this method allows for broad alkene substrate scope, excellent regio- and enantioselectivities, scalabilities and a wide array of applications, and provides a useful route for the convenient and straightforward synthesis of chiral β-hydroxy alkylcarboxylic acids/esters. This result is published in ACIE. Congratulations Bing Tian.
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Palladium-catalysed enantioselective diacetoxylation of terminal alkenes
A Pd(II)-catalysed enantioselective diacetoxylation of terminal alkenes, including challenging substrates such as 1-propene and 1-butene was reported. Notably, ligand engineering of the simple pyridinyl oxazoline ligand is essential for substantially increasing the catalytic reactivity of Pd(OAc)2. The method allowed precise asymmetric diacetoxylation reactions from feedstock alkenes to complex molecules bearing multiple alkenic moieties, which provides rapid and efficient access to various synthetically useful chiral 1,2-diols. This result is published in Nat. Catal. Congratulations Bing Tian.
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Anionic Bisoxazoline Ligands Enable Copper-Catalyzed Asymmetric Radical Azidation of Acrylamides
Asymmetric radical azidation for the synthesis of chiral alkylazides remains a tremendous challenge in organic synthesis. We report here an unprecedented highly enantioselective radical azidation of acrylamides catalyzed by 1？mol？% of a copper catalyst. The substrates were converted to the corresponding alkylazides in high yield with good‐to‐excellent enantioselectivity. This result is published in ACIE. Congratulations Lianqian Wu and Dunqi Wu.
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Enantioselective Copper-Catalyzed Trifluoromethylation of Benzylic Radicals via Ring Opening of Cyclopropanols
The asymmetric trifluoromethylation of aryl-substituted cyclopropanols via a radical ring-opening pathway is reported herein, which provides an easy and straightforward access to structurally diverse β-CF3 ketones in good yields and excellent enantioselectivities under very mild conditions. This result is published in Chem. Congratulations Chao Jiang.
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Asymmetric Coupling of Carbon-Centered Radical Adjacent to Nitrogen: Copper-Catalyzed Cyanation and Etherification of Enamides
The first copper-catalyzed asymmetric cyanation and etherification of enamides have been established, where a carbon-centered radical adjacent to a nitrogen atom (CRAN) is enantioselectively trapped by a chiral copper (II) species. This result is published in ACIE. Congratulations Guoyu Zhang and Song Zhou.
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Enantioselective Copper-Catalyzed Alkynylation of Benzylic C-H Bonds via Radical Relay
The first enantioselective alkynylation of benzylic C-H bonds via copper-catalyzed radical relay has been established, which provides an easy access to structurally diverse benzylic alkynes in good yields with excellent enantioselectivities. This result is published in JACS. Congratulations Liang Fu.
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Palladium(II)-Catalyzed Enantioselective Azidation of Unactivated Alkenes
The first Pd-catalyzed enantioselective azidation of unactivated alkenes using readily accessible 1‐azido‐1,2‐benziodoxol‐3(1H)‐one (ABX) as an azidating source has been established, which affords a wide variety of structurally diverse 3‐N3‐substituted piperidines in good yields with excellent enantioselectivities. Notably, the employment of both an electrophilic azidating reagent and the sterically bulky chiral pyridinyl‐oxazoline (Pyox) ligand is crucial to the successful reaction. This result is published in ACIE. Congratulations Xiaonan.
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Enantioselective Pd(II)-Catalyzed Oxidative Aminofluorination of Unactivated Alkenes Using Et4NF·3HF as a Fluoride Source
The first asymmetric Pd(II)-catalyzed aminofluorination of unactivated alkenes using chiral quinolone-oxazolines (Quox) as ligand has been developed, which provides an easy access to a wide array of enantiomerically enriched β‐fluoropiperidines in good yields with excellent enantioselectivities. Notably, Et4NF·3HF as a readily accessible nucleophilic fluoride source was found to play an essential role in the enantioselective control, and CsOCF3 also acts a key additive to improve the excellent ee value of products. This result is published in ACIE. Congratulations Chuanqi.
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Congratulations
Congratulations to Lianqian Wu(吴联谦) and Xiang Li(李响) on obtaining their PhD degree.
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Welcome
Welcome Dr. Weigang Fan from Université de Lyon, INSA Lyon (France) to join our group as a Postdoc.
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Proton-Coupled Electron Transfer Enables Tandem Radical Relay for Asymmetric Copper-Catalyzed Phosphinoylcyanation of Styrenes
A tandem radical relay strategy was realized for the first Cu(I)-catalyzed enantioselective phosphinocyanation of styrenes. In this reaction, tBuOOSiMe3 generated in situ from tBuOOH serves as a radical initiator to trigger t-butoxy radical production upon oxidization of L*Cu(I) species via proton-coupled-electron transfer (PCET) pathway, which leads to sequential phosphinoyl radical and benzyl radical formations. This result is published in Org Lett. Congratulations Guoyu Zhang.
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Enantioselective Arylation of Benzylic C-H bonds via CopperCatalyzed Radical Relay
A novel enantioselective Cu-catalyzed arylation of benzylic C-H bonds using alkylarenes as a limiting reagent has been developed, where a chiral bisoxazoline ligand bearing an acetate ester moiety plays a key role in both reactivity and enantioselectivity. The reaction provides an efficient access to various chiral 1,1- diarylalkanes in good yields with good to excellent enantioselectivities, and displays excellent functional group tolerance. This result is published in ACIE. Congratulations Wen Zhang.
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Enantioselective Construction of Quaternary All-Carbon Centers via Copper-Catalyzed Arylation of Tertiary Carbon-Centered Radicals
An enantioselective copper-catalyzed arylation of tertiary carbon-centered radicals, leading to quaternary all-carbon stereocenters, has been developed. The tertiary carbon-centered radicals, including both benzylic and nonbenzylic radicals, were produced by the addition of trifluoromethyl radical to α-substituted acrylamides, and subsequently captured by chiral aryl copper(II) species to give C？Ar bonds with excellent enantioselectivity. This result is published in JACS. Congratulations Lianqian Wu.
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Palladium(II)-Catalyzed Enantioselective Aminotrifluoromethoxylation of Unactivated Alkenes using CsOCF3 as a Trifluoromethoxide Source
Asymmetric Pd(II)-catalyzed intramolecular aminotrifluoromethoxylation of unactivated alkenes using readily accessible and stable CsOCF3 as a trifluoromethoxide source has been developed, which affords a wide variety of enantiomerically enriched β-substituted OCF3-containing piperidines in good yields. This result is published in ACIE . Congratulations Chaohuang Chen.
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Pd-Catalyzed Intermolecular Arylcarbonylation of Unactivated Alkenes: Incorporation of Bulky Aryl at Room Temperature
A Pd-catalyzed intermolecular arylcarbonylation of unactivated alkenes has been established herein. Unsymmetric diaryliodonium salts (DAIS) are used as arylation reagents, in which the bulky aryls (ArL) are exclusively incorporated into the arylcarbonylated products bearing the ArL group and a carboxylic ester group at the α- and？β-carbon position on the terminal C-C double bond, respectively. This result is published in ACIE. Congratulations Xiang Li.
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Enantioselective Trifluoromethylalkynylation of Alkenes via Copper-Catalyzed Radical Relay
A novel enantioselective copper-catalyzed trifluoromethylalkynylation of styrenes, proceeding through a radical relay process, is described herein, which affords structurally diverse CF3-containing propargylic compounds in good yield with excellent enantioselectivities under very mild conditions. In addition, the reaction features wide substrate scope and good functional group tolerance. Moreover, the trifluoromethylalkynylated products can be easily converted into synthetically useful chiral terminal alkynes, allenes, Z-alkenes, as well as CF3-modified nonsteroidal anti-inflammatory drugs. This result is published in JACS. Congratulations Liang Fu.
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Copper-Catalyzed Radical Relay for Asymmetric Radical Transformations
We present our recent studies on the enantioselective induction of prochiral benzylic radicals using a chiral bisoxazoline (Box)/Cu catalytic system as part of the Accounts of Chemical Research special issue “Hydrogen Atom Transfer”. Congratulations Fei Wang.
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Welcome
Welcome Xintuo Yang to our group as a PhD candidate, who got his MS degree at Chengdu Institute of Organic Chemistry, CAS.
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Enantioselective Pd(II)-Catalyzed Intramolecular Oxidative 6-endo Aminoacetoxylation of Unactivated Alkenes
A novel asymmetric 6-endo aminoacetoxylation of unactivated alkenes by palladium catalysis, which yields chiral β-acetoxylated piperidines with excellent chemo-, regio- and enantioselectivities under very mild reaction conditions, has been established herein by employing a new designed pyridine-oxazoline (Pyox) ligand. Importantly, introducing a sterically bulky group into the C-6 position of Pyox is crucial to enhance the reactivity of the amino-acetoxylation of alkenes. This result is published in JACS. Congratulations XIaoxu.
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Divergent Synthesis of CF3-Substituted Allenyl Nitriles by Ligand-Controlled Radical 1,2- and 1,4-Addition of 1,3-Enynes
A ligand-controlled radical 1,2- and 1,4-addition of 1,3-enynes has been developed, which provides an access to a variety of CF3-containing tri- and tetra-substituted allenyl nitriles. The reaction features broad substrate scope and excellent functional group compatibility. Moreover, this protocol represents a novel regioselectivity-tunable functionalization of 1,3-enynes via radicals. This result is published in ACIE. Congratulations Fei & Dinghai.
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Regioselective Palladium-Catalyzed C-H Bond Trifluoroethylation of Indoles: Exploration and Mechanistic Insight
A selective palladium-catalyzed trifluoroethylation reaction of indoles has been developed. The C-H bond activation process, using CF3CH2I as the fluoroalkyl source, can be employed to prepare a variety of 2-CF3CH2 substituted indoles. The results of a preliminary mechanistic study and DFT calculations show that a β-diketone, acting as an ionic palladium ligand, plays an important role in governing the efficiency of the palladium-catalyzed trifluoroethylation reaction by accelerating the oxidative addition step. In contrast, transfer of the indole N-H proton in the palladium center is involved in the rate-determining step. This result is published in ACS Catal. Congratulations Hao.
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Welcome
Welcome Philipp.Pflüger from University of Münster(Germany) to our group for research internship.
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Welcome
Welcome Dr. TianBing(田兵) to our group as a Postdoc, who got his PhD at Heidelberg University(Germany).
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Palladium-Catalyzed Intermolecular Ditrifluoromethoxylation of Unactivated Alkenes: CF3O？Palladation Initiated by Pd(IV)
A novel palladium-catalyzed intermolecular ditrifluoromethoxylation of unactivated alkenes has been developed, using a new electrophilic reagent, SelectfluorCN, as a strong oxidant, and AgOCF3 as a trifluoromethoxide source. Preliminary mechanistic studies revealed that the reaction was possibly initiated by Pd(IV) species, and an unusual cis-addition of CF3O？Pd(IV) into the double bond leads to the formation of the first C？OCF3 bond; in addition, the second C？OCF3 bond was produced through reductive elimination at high-valent palladium center. Congratulations to Chaohuang Chen.
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Awards Notification
Congratulations to Wen Zhang(张文) to win the "Special Prize of the Presidential Scholarship of Chinese Academy of Sciences(中国科学院院长特别奖)".
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Enantioselective Decarboxylative Cyanation Employing Cooperative Photoredox Catalysis and Copper Catalysis
The merger of photoredox catalysis with asymmetric copper catalysis have been realized to convert achiral carboxylic acids into enantiomerically enriched alkyl nitriles. Under mild reaction condition, the reaction exhibits broad substrate scope, high yields and high enantioselectivities. Furthermore, the reaction can be scaled up to synthesize key chiral intermediates to bioactive compounds. Congratulations to Dinghai Wang.
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Palladium-Catalyzed Intermolecular Azidocarbonylation of Alkenes via a Cooperative Strategy
We have developed a novel intermolecular β-azidocarbonylation reaction of alkenes, in which a combination of iodine(III)-mediated alkene activation and palladium-catalyzed carbonylation was demonstrated as an efficient strategy for the difunctionalization of alkenes. A variety of ？-azido carboxylic esters were obtained from mono- and 1,1-disubstituted terminal alkenes with excellent regioselectivities. In addition, the introduced azido group can be reduced to amine group, providing a facile access to β-amino acid derivatives from simple olefins. This result is published in JOC. Congratulations to Ming Li and Feng Yu.
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Palladium-Catalyzed Intermolecular Oxidative Fluorocarbonylation of Unactivated Alkenes: Efficient Access of β-Fluorocarboxylic esters
We have developed a novel palladium-catalyzed and iodine (III)-mediated intermolecular fluorocarbonylation of alkenes with a cooperative strategy. The employment of iodoarene difluorides as the oxidant and fluoride source is crucial for the successful catalytic transformation. The current transformation presents the first convenient method to generate β-fluorinated carboxylic acid derivatives under mild reaction conditions from simple alkenes with excellent regioselectivity. .This result is published in ACIE. Congratulations Xiaoxu.
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Awards Notification
Due to the excellent work, Dr. Fei Wang has won the "2017 Reaxys PhD Prize", Congratulate him.
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Congratulations
Congratulations to Zhaoli Liang(梁兆利), Chaohuang Chen(陈朝煌) and Dinghai Wang(王定海) to obtain their doctorate degrees.
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Catalytic Oxidative Trifluoromethoxylation of Allylic C-H Bonds using a Palladium Catalyst
We have developed a novel catalytic intermolecular allylic C-H trifluoromethoxylation of alkenes using a palladium catalyst, in which CsOCF3 was employed as the trifluoromethoxide source and BQ as the oxidant. This reaction provides an efficient route for directly accessing allylic trifluoromethoxy ether derivatives with excellent regioselectivities from terminal alkenes via an allylic C-H bond activation process.This result is published in ACIE. Congratulations Xiaoxu.
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Copper-Catalyzed Arylation of Benzylic C–H bonds with Alkylarenes as the Limiting Reagents
Based on the concept of our Science paper, we have developed a novel copper-catalyzed arylation of benzylic C–H bonds with nucleophilic arylboronic acids that provides an efficient way to synthesize various 1,1-diarylalkanes with a broad substrate scope and excellent functional group compatibility. The reactions occur at room temperature using alkylarenes as the limiting reagents, which allows access to the arylation of the more valuable and complex bioactive compounds. This result is published in JACS. Congratulations Wen Zhang.
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Asymmetric Copper-Catalyzed Intermolecular Aminoarylation of Styrenes: Efficient Access to Optical 2,2-diarylethylamines
We have developed a copper-catalyzed enantioselective intermolecular aminoarylation of alkenes using a novel N-fluoro-N-alkylsulfonamide as the amine reagent, which could react with the Cu(I) catalyst to release a related amino radical. Varieties of optical 2,2-diaryl-ethylamines were efficient synthesized from simple styrenes with high enantioselectivity, and these products can serve as valuable synthons toward bioactive molecules synthesis. This result is published in JACS. Congratulations Dinghai.
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Welcome
Welcome Dr. Liang Fu to our group as a Postdoc, who got his PhD at RWTH Aachen University (Germany).
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Awards Notification
Due to their excellent works, Dinghai Wang has won the honor of “Shanghai Outstanding Graduates”(上海市优秀毕业生)；Wen Zhang has won the honor of “Good Student Model”(三好学生标兵)；Lianqian Wu has won the honor of “Outstanding Student” (优秀学生). Congratulations them.
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Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N-H and Aryl C-H Bond Cleavage
We have developed an asymmetric palladium-catalyzed intramolecular oxidative aminoarylation of alkenes with quinoline–oxazoline chiral ligands and Ag2CO3 as the oxidant. Various indolines containing a quaternary stereogenic center were synthesized in high yield with excellent enantioselectivity. This result is published in ACIE. Congratulations Wen.
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Asymmetric Cu-Catalyzed Intermolecular Trifluoromethylarylation of Styrenes: Enantioselective Arylation of Benzylic Radicals
Based on the radical relay strategy, we have developed a novel asymmetric radical trifluoromethyl-arylation of alkenes, in which which provides an efficient approach to access chiral CF3-containing 1,1-diarylmethane derivatives with good to excellent enantioselectivity. Various vinyl arenes and aryl boronic acids are compatible with these conditions. The utility of the method is demonstrated by accessing modified bioactive molecules. This result is published in JACS. Congratulations Lianqian.
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Enantioselective Copper-Catalyzed Intermolecular Amino- and Azido-cyanation of Alkenes via radical relay process
Based on the radical relay strategy, we have developed a novel enantioselective copper-catalyzed intermolecular amino- and azido-cyanation of alkenes, in which a variety of enantiomerically enriched β-amino/azido alkylnitriles were efficiently synthesized. And β-azido alkylnitriles could be converted to a series of highly valuable optical nitrogen-containing building blocks and bioactive compounds. This result is published in ACIE. Congratulations Dinghai.
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Enantioselective Copper-Catalyzed Intermolecular Cyanotrifluoromethylation of Alkenes via Radical Process
Based on the concept of our Science paper, we have developed a novel enantioselective copper-catalyzed intermolecular cyanotrifluoromethylation of alkenes, in which a variety of CF3-containing alkylnitriles are furnished with excellent enantiomeric excess. This result is published in JACS. Congratulations Fei Wang.
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Author Profile of Guosheng Liu in Angewandte Chemie
Prof Liu has published 10 articles in Angewandte Chemie in the last 10 years, and an author profile is presented. Congratulations Prof. Liu.
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Palladium(II)-Catalyzed Oxidative Difunctionalization of Alkenes: Bond Forming at a High-Valent Palladium Center
Difunctionalization of alkenes has emerged as a powerful transformation to greatly increase molecular complexity in organic synthesis with improved efficiency, which is a major research topic in our group. To summarize our work in the past nine years, we published a review in Acc. Chem. Res. In this account, we discuss our exploration and application of a “high-valent palladium strategy” for the synthesis of fluorine-containing organic molecules that are typically inaccessible from other methods, besides, hydrogen peroxide, which is an environmentally friendly oxidant, is also mentioned to oxidize alkyl C–Pd(II) species to form high-valent alkyl C–Pd intermediates. Congratulations Guoyin Yin, Xin Mu and Prof. Liu.
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Congratulations Wen and Fei.
Our lab, in collaboration with the Stahl's lab@ University of Wisconsin–Madison has developed a method for stereoselective functionalization of sp3-hybridized carbon–hydrogen [C(sp3)–H] bonds in complex organic molecules could facilitate much more efficient preparation of therapeutics and agrochemicals which is published in Science.
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Cooperative Strategy for the Highly Selective Intermolecular Oxycarbonylation Reaction of Alkenes using palladium catalyst
Our group has developed a novel method for intermolecular functionalization of terminal and internal alkenes in which hypervalent iodine, plays a key role by activating the alkene C=C bond for nuleophilic addition of the palladium catalyst. Utilizing the new approach, intermolecular oxycarbonylaton reactions of alkenes have been achieved and carried out under mild conditions to produce the corresponding β-oxycarbonylic acids with excellent efficiencies and levels of regio- and diastereo-selectivity. Congratulations Ming. [Angew. Chem. Int. Ed. 2016, 55, 10.1002/anie.201607248R1]
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Efficient Pathway for the Preparation of Aryl(isoquinoline)iodonium(III) Salts and Synthesis of Radiofluorinated Isoquinolines
Our lab, in collaboration with the Liang lab@ Massachusetts General Hospital and Harvard Medical School has developed a novel “one-pot” process to assemble aryl(isoquinoline)iodonium salts in 40–94%yields from mesoionic carbene silver complex and Aryl-IPy2(OTf)2. The method is general, practical, and compatible with well-functionalized molecules as well as useful for the preparation of a wide range of 18F-labeled isoquinolines resulting in up to 92% radiochemical conversion. Congratulations Zheliang.
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Postdoctoral positions are available immediately in the Prof. Liu’s lab. Interested candidates with strong experimental experience on organic chemisty, especially on radical chemistry and transition metal catalysis, please submit a cover letter, Curriculum Vitae (including 2x references) and a short research summary to Prof. Liu, gliu@mail.sioc.ac.cn. Please put "Applications - Liu Group - PostDoc" in the subject line.