about
An Unconventional Redox Cross Claisen Condensation-Aromatization of 4-Hydroxyprolines with Ketones.Synthesis of Aldehydes by Organocatalytic Formylation Reactions of Boronic Acids with Glyoxylic Acid.Orchestration of dual cyclization processes and dual quenching mechanisms for enhanced selectivity and drastic fluorescence turn-on detection of cysteine.Chemo- and Regioselective Organo-Photoredox Catalyzed Hydroformylation of Styrenes via a Radical Pathway.Rational Design of an Ultrasensitive and Highly Selective Chemodosimeter by a Dual Quenching Mechanism for Cysteine Based on a Facile Michael-Transcyclization Cascade Reaction.Aniline-Promoted Cyclization-Replacement Cascade Reactions of 2-Hydroxycinnamaldehydes with Various Carbonic Nucleophiles through In Situ Formed N,O-Acetals.Visible-Light-Promoted Nickel- and Organic-Dye-Cocatalyzed Formylation Reaction of Aryl Halides and Triflates and Vinyl Bromides with Diethoxyacetic Acid as a Formyl Equivalent.Correction: Synthesis of Z-alkenes via visible light promoted photocatalytic E → Z isomerization under metal-free conditions.Discovery of IDO1 and DNA dual targeting antitumor agents.Synthesis of Z-alkenes via visible light promoted photocatalytic E → Z isomerization under metal-free conditions.Direct Access of the Chiral Quinolinyl Core of Cinchona Alkaloids via a Brønsted Acid and Chiral Amine Co-catalyzed Chemo- and Enantioselective α-Alkylation of Quinolinylmethanols with Enals.Synthesis of Indolizines via Reaction of 2-Substitued Azaarenes with Enals by an Amine-NHC Relay Catalysis.Discovery of Novel Indoleamine 2,3-Dioxygenase 1 (IDO1) and Histone Deacetylase (HDAC) Dual Inhibitors.α-Functionalization of 2-Vinylpyridines via a Chiral Phosphine Catalyzed Enantioselective Cross Rauhut-Currier Reaction.Organocatalytic Asymmetric Formal [4 + 2] Cycloaddition of in Situ Oxidation-Generated ortho-Quinone Methides and Aldehydes.Co(OAc)2-Catalyzed Trifluoromethylation and C(3)-Selective Arylation of 2-(Propargylamino)pyridines via a 6-Endo-Dig Cyclization.Asymmetric synthesis of isoquinolinonaphthyridines catalyzed by a chiral Brønsted acid.Direct Cα-heteroarylation of structurally diverse ethers via a mild N-hydroxysuccinimide mediated cross-dehydrogenative coupling reaction.A dynamic kinetic asymmetric transfer hydrogenation-cyclization tandem reaction: an easy access to chiral 3,4-dihydro-2H-pyran-carbonitrilesSynthesis of Enantioenriched α-Deuterated α-Amino Acids Enabled by an Organophotocatalytic Radical ApproachFluorescent Detection of Dynamic H2O2/H2S Redox Event in Living Cells and OrganismsInvestigation of the Relationship Between H2O2 and HClO in Living Cells by a Bifunctional, Dual-ratiometric Responsive Fluorescent ProbeSynthesis of 2-Quinolinones via a Hypervalent Iodine(III)-Mediated Intramolecular Decarboxylative Heck-Type Reaction at Room TemperatureSmall Molecules Simultaneously Inhibiting p53-Murine Double Minute 2 (MDM2) Interaction and Histone Deacetylases (HDACs): Discovery of Novel Multitargeting Antitumor AgentsTrideuteromethylation Enabled by a Sulfoxonium Metathesis ReactionConstruction of N-Alkyl- and N-Arylaziridines from Unprotected Amines via C-H Oxidative Amination StrategyHighly stereoselective synthesis of aryl/heteroaryl-C-nucleosides via the merger of photoredox and nickel catalysisA naphthalimide-aminal-based pH-sensitive fluorescent donor for lysosome-targeted formaldehyde release and fluorescence turn-on readoutCopper Promoted Aerobic Oxidative C(sp3)-C(sp3) Bond Cleavage of N-(2-(Pyridin-2-yl)-ethyl)anilinesPotent Dual BET/HDAC Inhibitors for Efficient Treatment of Pancreatic CancerVisible-Light-Mediated, Chemo- and Stereoselective Radical Process for the Synthesis of C-Glycoamino AcidsOrganocatalytic Transformation of Aldehydes to Thioesters with Visible LightAnalyte Regeneration Fluorescent Probes for Formaldehyde Enabled by Regiospecific Formaldehyde-Induced Intramolecularity
P50
Q48057610-3E7CD101-A2A0-4F60-9241-1955B839C7B8Q48095489-41876416-EFA0-4BAC-8DF4-EEBFC29C7A1DQ48132781-B79C1979-B844-4EED-A89E-F9A126D79763Q48151904-1262620C-CDE5-4728-8DEB-FD33DEACA337Q48218113-3DE9C864-E96F-4292-B2C3-CE463719A2CDQ48221028-E07363E4-432E-43D9-9F4E-888DD3AB7539Q48374254-D95436B5-F0BD-431B-9BB0-5EC396DA3FCCQ48536375-E27E0C96-A1C8-4D98-8040-48D171C62786Q48589619-54AD5EEC-DF5F-4D83-9F8B-E01D45AB73A5Q49922491-900D2E82-1C1E-4B9D-ADEA-FCA541C8BF31Q50533349-98CB129F-353B-4F27-A9A5-0FCCA489AC6AQ50665717-CE485F2F-89E5-48F4-B247-6E55649AFF32Q52579088-86752CBB-20D9-4C83-91FF-CDDE51807F46Q52694144-257369A6-24BA-4818-B6BB-17282342D994Q52742849-B87493CC-ED4A-4896-9400-B812ED9C9833Q52802311-E5C16338-E6B6-4924-89CA-9C013519198CQ53146468-EB30482F-DD72-4985-9B08-E8D24085E8F1Q64901573-988E3922-E9B4-4981-886D-37690C9C32C1Q88119733-855A4570-D763-4BB6-830F-3A69722B9689Q89654769-5F8F0F2E-89EF-4242-8FD1-A92CBEEBBA0FQ89880435-F63C15D2-672E-47F2-AA30-2C0B90DA066DQ89979857-1B80037B-6DB5-4A9A-8C80-2F44423D3217Q90275135-F9DC9BE8-E3DF-48A2-9357-45958074437BQ90471887-B9CCFD6A-12DF-44EB-A0CD-AF39421E8048Q90921048-66F11970-7751-4265-8462-DEE8AD56AA70Q91276639-48BEC545-0961-489D-9AE3-F61A48AC1EB4Q91353632-18A99E03-E328-4B78-9D31-19FB9B57289FQ92387519-7580D7C7-28A4-4433-A8D1-7266FB3A243AQ92652078-E68B78FA-846F-49F0-BB33-D04BB6A742FEQ92678689-A45A0F99-926C-4F48-B7BC-7853A49518BEQ93054403-4093C9AA-8ECB-49E8-9D1B-ACDDF275F1A0Q93099375-0227136A-8EB7-4053-82B6-9E1CA12D83C4Q93239233-BB4D08A7-A03F-4F7C-9225-50D01685D4AC
P50
description
researcher (ORCID 0000-0001-6043-0860)
@en
name
Wei Wang
@en
type
label
Wei Wang
@en
prefLabel
Wei Wang
@en
P31
P496
0000-0001-6043-0860