A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.
about
Nickel-catalyzed C-O activation of phenol derivatives with potassium heteroaryltrifluoroborates.Condensation reactions to form oxazoline-substituted potassium organotrifluoroborates.Organotrifluoroborates and monocoordinated palladium complexes as catalysts--a perfect combination for Suzuki-Miyaura coupling.Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chloridesEfficient synthesis of substituted 3-azabicyclo[3.1.0]hexan-2-ones from 2-iodocyclopropanecarboxamides using a copper-free Sonogashira coupling.A method for the deprotection of alkylpinacolyl boronate esters.Rh(I)-catalyzed direct arylation of azines.Oxidative Heck Reactions using Aryltrifluoroborates and Aryl N-Methyliminodiacetic Acid (MIDA) BoronatesTandem Cycloisomerization/Suzuki Coupling of Arylethynyl MIDA BoronatesStructure-activity relationship study of pyridazine derivatives as glutamate transporter EAAT2 activators.Cross-coupling of mesylated phenol derivatives with potassium cyclopropyltrifluoroborate.Ru-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studiesAmphotericin primarily kills yeast by simply binding ergosterol.Synthesis of atropisomerically defined, highly substituted biaryl scaffolds through catalytic enantioselective bromination and regioselective cross-couplingA modified procedure for the palladium catalyzed borylation/Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides utilizing bis-boronic acid.From synthesis to function via iterative assembly of N-methyliminodiacetic acid boronate building blocks.Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts.A versatile catalyst system for Suzuki-Miyaura cross-coupling reactions of C(sp(2))-tosylates and mesylates.DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions.MIDA boronates are hydrolysed fast and slow by two different mechanisms.A Divalent Protecting Group for Benzoxaboroles.Palladium-catalyzed transformations of salvinorin A, a neoclerodane diterpene from Salvia divinorum.Development of a Suzuki cross-coupling reaction between 2-azidoarylboronic pinacolate esters and vinyl triflates to enable the synthesis of [2,3]-fused indole heterocycles.Selection of boron reagents for Suzuki-Miyaura coupling.Pinene-derived iminodiacetic acid (PIDA): a powerful ligand for stereoselective synthesis and iterative cross-coupling of C(sp3) boronate building blocks.Linchpin dienes: key building-blocks in the synthesis of polyenic frameworks.Design, Synthesis, and Validation of an Effective, Reusable Silicon-Based Transfer Agent for Room-Temperature Pd-Catalyzed Cross-Coupling Reactions of Aryl and Heteroaryl Chlorides with Readily Available Aryl Lithium Reagents.Synthesis and Utility of Dihydropyridine Boronic Esters.Stereospecific Ni-catalyzed cross-coupling of potassium alkenyltrifluoroborates with alkyl halides.Acylboranes: synthetic strategies and applications.Transforming Suzuki-Miyaura cross-couplings of MIDA boronates into a green technology: no organic solvents.Cross-electrophile coupling: principles of reactivity and selectivityA simple, multidimensional approach to high-throughput discovery of catalytic reactions.Chemoselective boronic ester synthesis by controlled speciation.3-Cyanoallyl boronates are versatile building blocks in the synthesis of polysubstituted thiophenes.A new palladium precatalyst allows for the fast Suzuki-Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic acids.Nickel-catalyzed cross-coupling of potassium aryl- and heteroaryltrifluoroborates with unactivated alkyl halides.Total synthesis of synechoxanthin through iterative cross-coupling.Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid
P2860
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P2860
A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
A general solution for unstabl ...... rom air-stable MIDA boronates.
@en
A general solution for unstabl ...... rom air-stable MIDA boronates.
@nl
type
label
A general solution for unstabl ...... rom air-stable MIDA boronates.
@en
A general solution for unstabl ...... rom air-stable MIDA boronates.
@nl
prefLabel
A general solution for unstabl ...... rom air-stable MIDA boronates.
@en
A general solution for unstabl ...... rom air-stable MIDA boronates.
@nl
P2093
P356
P1476
A general solution for unstabl ...... rom air-stable MIDA boronates.
@en
P2093
David M Knapp
Eric P Gillis
Martin D Burke
P304
P356
10.1021/JA901416P
P407
P577
2009-05-01T00:00:00Z