Aqueous-phase, palladium-catalyzed cross-coupling of aryl bromides under mild conditions, using water-soluble, sterically demanding alkylphosphines.
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Design and synthesis of a 3'-O-allyl photocleavable fluorescent nucleotide as a reversible terminator for DNA sequencing by synthesisSelective 5-hydroxytryptamine 2C receptor agonists derived from the lead compound tranylcypromine: identification of drugs with antidepressant-like action.Storable arylpalladium(II) reagents for alkene labeling in aqueous media.Pd/C-catalyzed, copper-free Sonogashira coupling: one-pot synthesis of 1-aryl-4-(2-phenylethynyl)[1,2,4]triazolo[4,3-a]quinoxalines in water.An efficient Pd-NHC catalyst system in situ generated from Na2PdCl4 and PEG-functionalized imidazolium salts for Mizoroki-Heck reactions in water."Designer"-Surfactant-Enabled Cross-Couplings in Water at Room TemperatureKeggin type mono Ni(II)-substituted phosphomolybdate: a sustainable, homogeneous and reusable catalyst for Suzuki-Miyaura cross-coupling.Coulombic inter-ligand repulsion effects on the Pt(II) coordination chemistry of oligocationic, ammonium-functionalized triarylphosphines.The Design of Ligand Systems for Immobilisation in Novel Reaction MediaFacile palladium catalyzed Suzuki–Miyaura coupling in air and water at ambient temperatureCross-Coupling Reactions in Aqueous MediaMetal-Catalyzed Cross-Couplings of Aryl Halides to Form C-C Bonds in Aqueous MediaImidazolium ionic liquid-tagged palladium complex: an efficient catalyst for the Heck and Suzuki reactions in aqueous media
P2860
Q31159921-A6AEBD99-14F3-4652-BD14-ADF16AD727C6Q34962263-88B42187-3713-44B6-BCB1-FE52556BD19FQ38642190-A67E33B9-FACC-4AA0-A746-2ACA18970A16Q40745793-4896C1A3-63A0-49CE-AB65-D09A6A1814EFQ41594190-C7C77405-104B-4A43-B776-A1075FC5D6C3Q41766928-F7902AA9-1B9B-4F4D-9074-71F1056FF85FQ44123264-534417D6-B246-4901-A5D0-024D818DCE57Q52714815-8940B878-924B-4CA4-AE04-B6A289406300Q57340437-80F59BBA-0A77-45D5-B120-53F3C6CBF847Q57907963-B3BC5F95-21EA-4B62-9A07-DA7CA60959E4Q57946335-E75849F4-80BF-41BD-90B2-1E5979990996Q57946344-4E1B6C13-0C04-432C-87BD-7EA44F65D36CQ58200710-329AD02D-09A5-47BD-A810-F79E2308A2F2
P2860
Aqueous-phase, palladium-catalyzed cross-coupling of aryl bromides under mild conditions, using water-soluble, sterically demanding alkylphosphines.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
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2004年学术文章
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2004年學術文章
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name
Aqueous-phase, palladium-catal ...... lly demanding alkylphosphines.
@en
Aqueous-phase, palladium-catal ...... lly demanding alkylphosphines.
@nl
type
label
Aqueous-phase, palladium-catal ...... lly demanding alkylphosphines.
@en
Aqueous-phase, palladium-catal ...... lly demanding alkylphosphines.
@nl
prefLabel
Aqueous-phase, palladium-catal ...... lly demanding alkylphosphines.
@en
Aqueous-phase, palladium-catal ...... lly demanding alkylphosphines.
@nl
P356
P1476
Aqueous-phase, palladium-catal ...... lly demanding alkylphosphines.
@en
P2093
Lucas R Moore
Rebecca B DeVasher
P304
P356
10.1021/JO048910C
P407
P577
2004-11-01T00:00:00Z