about
Dolichol biosynthesis and its effects on the unfolded protein response and abiotic stress resistance in Arabidopsis.Built-in 5-aminooxazole as an internal activator of the terminal carboxylic acid: an alternative access to macrocyclodepsipeptides.Access to macrocycles with an endo aryl ether and an endo aryl-aryl bond, development and application.To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis.Simulation of fruit-set and trophic competition and optimization of yield advantages in six Capsicum cultivars using functional-structural plant modelling.Hybridization of long pyridine-dicarboxamide oligomers into multi-turn double helices: slow strand association and dissociation, solvent dependence, and solid state structures.Copper-promoted N-cyclopropylation of anilines and amines by cyclopropylboronic acid.Passerini three-component reaction of alcohols under catalytic aerobic oxidative conditions.Total synthesis of complestatin (chloropeptin II).Efficient synthesis of alpha-ketoamides via 2-acyl-5-aminooxazoles by reacting acyl chlorides and alpha-isocyanoacetamides.Activation of a terminal carboxylic acid by an internal oxazole: a novel synthesis of macrocyclodepsipeptide.Tertiary amines as synthetic equivalents of vinyl cations: zinc bromide promoted coupling of propargylamines with α-isocyanoacetamides to give 2,4,5-trisubstituted oxazoles initiated by an internal redox process.Chiral Brønsted acid-catalyzed enantioselective three-component Povarov reaction.Synthesis of multifunctionalized 1,2,3,4-tetrahydropyridines, 2,3-dihydropyridin-4(1H)-ones, and pyridines from tandem reactions initiated by [5+1] cycloaddition of N-formylmethyl-substituted enamides to isocyanides: mechanistic insight and synthetiCooperative Pd/Cu Catalysis: Multicomponent Synthesis of Tetrasubstituted Imidazolones from Methyl α-Isocyanoacetates, Primary Amines, and Aryl(vinyl) Iodides.Highly enantioselective aza Morita-Baylis-Hillman reaction catalyzed by bifunctional beta-isocupreidine derivatives.Ketenimines from Isocyanides and Allyl Carbonates: Palladium-Catalyzed Synthesis of β,γ-Unsaturated Amides and Tetrazoles.Mild oxidative one-carbon homologation of aldehyde to amide.Copper-mediated N-cyclopropylation of azoles, amides, and sulfonamides by cyclopropylboronic acid.Synthetic studies toward ecteinascidin 743.Palladium(II)-catalyzed cyclizative cross-coupling of ortho-alkynylanilines with ortho-alkynylbenzamides under aerobic conditions.Asymmetric total synthesis of (-)-quinocarcin.Palladium-catalyzed intramolecular C-arylation of benzylic carbon: synthesis of 3-benzoxazolylisoindolinones by a sequence of Ugi-4CR/postfunctionalization.Mechanistic study on the palladium(II)-catalyzed synthesis of 2,3-disubstituted indoles under aerobic conditions: anion effects and the development of a low-catalyst-loading process.Palladium-Catalyzed Enantioselective Desymmetrizing Aza-Wacker Reaction: Development and Application to the Total Synthesis of (-)-Mesembrane and (+)-Crinane.Catalytic Enantioselective Double Carbopalladation/C-H Functionalization with Statistical Amplification of Product Enantiopurity: A Convertible Linker Approach.Silver Nitrate-Catalyzed Isocyanide Insertion/Lactamization Sequence to Imidazolones and Quinazolin-4-ones: Development and Application in Natural Product Synthesis.Copper-Catalyzed Enantioselective Domino Arylation/Semipinacol Rearrangement of Allylic Alcohols with Diaryliodonium Salts.α-Oxo-Ketenimines from Isocyanides and α-Haloketones: Synthesis and Divergent Reactivity.Copper-Catalyzed Three-Component Carboazidation of Alkenes with Acetonitrile and Sodium Azide.Palladium-Catalyzed Enantioselective Narasaka-Heck Reaction/Direct C-H Alkylation of Arenes: Iminoarylation of Alkenes.Silver-Catalyzed Three-Component 1,1-Aminoacylation of Homopropargylamines: α-Additions for Both Terminal Alkynes and Isocyanides.Organocatalytic Enantioselective Acyloin Rearrangement of α-Hydroxy Acetals to α-Alkoxy Ketones.Copper-Catalyzed Enantioselective Arylative Desymmetrization of Prochiral Cyclopentenes with Diaryliodonium Salts.Fluorophores for Excited-State Intramolecular Proton Transfer by an Yttrium Triflate Catalyzed Reaction of Isocyanides with Thiocarboxylic Acids.Organocatalytic Nucleophilic Addition of Hydrazones to Imines: Synthesis of Enantioenriched Vicinal Diamines.Nomenclature for HKT transporters, key determinants of plant salinity tolerance.Catalytic Asymmetric Tandem Reaction of Tertiary Enamides: Expeditious Synthesis of Pyrrolo[2,1-a]isoquinoline Alkaloid Derivatives.Water as a Hydride Source in Palladium-Catalyzed Enantioselective Reductive Heck Reactions.Unified strategy to monoterpene indole alkaloids: total syntheses of (±)-goniomitine, (±)-1,2-dehydroaspidospermidine, (±)-aspidospermidine, (±)-vincadifformine, and (±)-kopsihainanine A.
P50
Q30844995-1319AEA2-0259-41A9-8E00-85E4732E8E74Q34057299-B89157BD-5FB9-4F51-8EE1-B138FE63D5C2Q37870118-199C7B99-BB45-418D-BAB4-B2F7B56A9396Q38781937-DF1334EE-8CF5-475D-BC49-8AD74563AFF3Q41761271-1BEC5475-F095-4811-8728-08FB6FA60B2CQ43106271-5AA38431-623F-4B2F-8D13-E6560F22338BQ43111370-895BCAD6-DD4A-4C39-BBEF-659B9E7BDA61Q43135556-8B99F870-E551-4D9C-AB96-80DAE6454A0FQ43165698-30CF7CCB-779D-46D0-9FFD-D614FC7F7167Q43188824-50E3044E-290A-41EA-AD14-9E4EDEA24437Q43663198-5767AB1F-930F-49C3-A584-C360100FC2CBQ44383795-525EE27F-0B20-43F0-B3C4-513C8FB3F1DBQ46067458-76C49CB7-582C-4CF9-BEAB-DBF7619537CAQ46195640-D607EC3A-1CB2-4482-8B99-428914A72291Q46242274-F198A020-3EA3-4FB7-A4C1-B8DF2035B2EBQ46409438-561C1B6C-6AE8-43A6-9037-10F422728AA2Q46457738-4EAFBE1E-C565-4536-834C-A54FB7E19CCBQ46482775-CED3FF62-38F3-4DB1-835E-EB7BE9CF0184Q46495240-EB874C17-F3A2-4E0A-9CF7-03C27B7BE0DCQ46498561-1BF40376-B47C-4E13-BDF9-BD2BEB167574Q46549471-B3078B8E-A6DA-484A-A634-0D4E63FE34F8Q46613579-4ABF610B-DCFF-4EF7-8754-075F84556253Q46670912-C0872926-5627-475F-A92A-21F4A7E9BCAFQ46853925-C2E259F3-F765-4C86-99D9-43574D728A47Q47190658-0DC69A56-F07E-45E7-A303-500843DC639BQ47663178-CD35C96E-4DAD-411D-B58A-C2F9CBD2C07DQ47754339-F404A431-E170-4E38-BA4D-114449C43EE1Q47863934-45F8B22D-7F7B-4FDE-B6B7-536C3A0FF779Q47867502-50F0979F-4AB9-479E-AFD9-6C213226E210Q47985816-CA18640F-1DBF-41A9-8D8F-2A81C2A6C4C7Q48011897-BCBC14EB-2EAE-4C9A-8450-D36493EA859CQ48159063-ED814323-5967-423C-83DA-AA799BE6CF52Q48241798-9CDA147E-3BF5-4E71-8514-E71C7E212E34Q48261381-4C289CB9-29EF-45EA-92ED-4EC834687A66Q48277699-7533AC29-9D7E-4261-8C77-0B55E70BCC9FQ48296855-081C272E-11AA-4F59-9CDA-5787A2A78AF9Q48701259-A2D94C0E-DF6B-4FA6-9069-1173A11E0004Q50880083-B8DAAB83-45F1-49CF-AC28-6FF855C6D7D6Q50970232-842565CC-5676-4087-9789-E2A84A4EB5D2Q51048339-6D2CFF3C-1959-4590-99A9-79B89BF97789
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jieping Zhu
@ast
Jieping Zhu
@en
Jieping Zhu
@es
Jieping Zhu
@nl
Jieping Zhu
@sl
type
label
Jieping Zhu
@ast
Jieping Zhu
@en
Jieping Zhu
@es
Jieping Zhu
@nl
Jieping Zhu
@sl
prefLabel
Jieping Zhu
@ast
Jieping Zhu
@en
Jieping Zhu
@es
Jieping Zhu
@nl
Jieping Zhu
@sl
P1053
E-8524-2015
P106
P31
P3829
P496
0000-0002-8390-6689