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A Facile Radiolabeling of [18F]FDPA via Spirocyclic Iodonium Ylides: Preliminary PET Imaging Studies in Preclinical Models of NeuroinflammationTBHP/TBAI-Mediated Oxidative Cascade Reaction Consisting of Dimerization, Cyclization, and 1,2-Aryl Migration: Metal-Free Synthesis of Pyrrolin-4-ones and Highly Substituted Pyrroles.PhI(OCOCF3)2-Mediated Construction of a 2-Spiropseudoindoxyl Skeleton via Cascade Annulation of 2-Sulfonamido-N-phenylpropiolamide Derivatives.In Vitro and in Vivo Evaluation of 11C-Labeled Azetidinecarboxylates for Imaging Monoacylglycerol Lipase by PET Imaging Studies.Synthesis of trifluoromethylated 2H-azirines through Togni reagent-mediated trifluoromethylation followed by PhIO-mediated azirination.Iodocyclization of N-Arylpropynamides Mediated by Hypervalent Iodine Reagent: Divergent Synthesis of Iodinated Quinolin-2-ones and Spiro[4,5]trienonesCorrection to Construction of 2-Arylbenzo[4,5]thieno[2,3-d]thiazole Skeleton via CuCl/S-Mediated Three-Component ReactionRegioselective Chlorolactonization of Styrene-Type Carboxylic Esters and Amides via PhICl2-Mediated Oxidative C-O/C-Cl Bond FormationsSynthesis of Spirooxindoles from N-Arylamide Derivatives via Oxidative C(sp2)-C(sp3) Bond Formation Mediated by PhI(OMe)2 Generated in SituCascade Synthesis of Benzothieno[3,2- b]indoles under Oxidative Conditions Mediated by CuBr and tert-Butyl HydroperoxideIn Situ Formation of RSCl/ArSeCl and Their Application to the Synthesis of 4-Chalcogenylisocumarins/Pyrones from o-(1-Alkynyl)benzoates and ( Z)-2-Alken-4-ynoatesLactonization of 2-Alkynylbenzoates for the Assembly of Isochromenones Mediated by BF3·Et2OSynthesis of 4-Chloroisocoumarins via Intramolecular Halolactonization of o-Alkynylbenzoates: PhICl2-Mediated C-O/C-Cl Bond FormationConstruction of 2-Arylbenzo[4,5]thieno[2,3-d]thiazole Skeleton via CuCl/S-Mediated Three-Component ReactionReplacement of Protein Binding-Site Waters Contributes to Favorable Halogen Bond Interactions
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Q41556036-B28B3D60-047B-4232-9B46-CABD34F76C28Q48165817-D88D0ABA-3B74-4C31-B552-6E20DC1B62ECQ51025117-7AA67EB2-2C71-4E1C-A88F-CC638D091E9BQ52315796-E8ACB002-673D-44BA-8E07-FBB80AD171BEQ55440554-E00CC7C3-B639-47C2-B92A-A013B93F9585Q89179317-E14A7DCE-E132-4E24-88C5-263A57AEC956Q89568848-7E946D93-0A59-41BC-91DE-B6B7B23AAA92Q90126040-FC2742E6-327F-401F-98A1-3DBC0215BE4DQ91276625-8E095492-F692-40A3-97AA-96BA0037B6AAQ91423465-2682393C-7737-43FD-BDA1-1D4EF256C7DCQ91725193-AA418F04-88E1-4084-ADDF-2A879BAD3B6FQ92067198-D9F46C33-D95D-4A74-9F15-D23EE3019DB9Q92323484-089BA1F4-0E8B-49A8-B0B7-86399DD1F620Q92371038-DCF9FF4E-0D03-42D3-9369-15EBC8A7E8A9Q92678632-5E139E91-5D6D-418A-A7BC-EFAA40D68D5A
P50
description
researcher
@en
wetenschapper
@nl
name
Yunfei Du
@en
Yunfei Du
@nl
type
label
Yunfei Du
@en
Yunfei Du
@nl
prefLabel
Yunfei Du
@en
Yunfei Du
@nl
P31
P496
0000-0002-0213-2854