About: A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks

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article by Eric P. Gillis & Martin D. Burke published May 2007 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2007 (uk) article scientifique publié en 2007 (fr) im Mai 2007 veröffentlichter wissenschaftlicher Artikel (de) article by Eric P. Gillis & Martin D. Burke published May 2007 in Journal of the American Chemical Society (en)
publication date	wds:Q56681309-A23CEBE2-5688-492B-92EB-5FC4CE089BC3
publication date	2007-05-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56681309-59336AC3-490A-46AD-A608-F7A9B83E7FF7
language of work or name	English
author name string	wds:Q56681309-79607451-5607-4CB0-9EE3-17CAB16669F8 wds:Q56681309-CCCBE82A-B44D-4A14-90A2-4FFEA26F9AF7
author name string	Martin D. Burke Eric P. Gillis
rdfs:label	A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks (en) A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks (nl)
skos:prefLabel	A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks (en) A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks (nl)
name	A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks (en) A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks (nl)
title	wds:Q56681309-443C0A35-E314-40B8-B155-54FD85F67E12
title	A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks (en)
page(s)	wds:Q56681309-CCBDCCAB-E1D8-4EC7-A8FA-212869DCED8E
page(s)	6716-6717
instance of	wds:Q56681309-1C98309F-4BA9-448E-B620-C5C383C939D2
instance of	scholarly article
PubMed ID	wds:Q56681309-8B9B3000-C50A-4782-A45C-E452C5E08D30
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17488084
PubMed ID	17488084
published in	wds:Q56681309-517530C4-BC79-45AE-A2DD-A33BD2CA7DD9
published in	Journal of the American Chemical Society
issue	wds:Q56681309-B4011F25-02CB-4142-8FF2-E0A417A7D036
volume	wds:Q56681309-BBAB60FA-D26F-4610-9E71-BAEB75BE63FE
issue	21
volume	129
DOI	wds:Q56681309-CC3B0D00-61FF-42A8-B11E-51EAACA7F4CE
DOI	http://dx.doi.org/10.1021/JA0716204
DOI	10.1021/JA0716204
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56681309
is cites work of	Stereoselective synthesis of dienyl-carboxylate building blocks: formal synthesis of inthomycin C. Replacing conventional carbon nucleophiles with electrophiles: nickel-catalyzed reductive alkylation of aryl bromides and chlorides Synthesis of many different types of organic small molecules using one automated process. Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. Cross-coupling Reactions of Organoboranes: An Easy Method for C–C Bonding Organotrifluoroborates and monocoordinated palladium complexes as catalysts--a perfect combination for Suzuki-Miyaura coupling Protecting group-free, selective cross-coupling of alkyltrifluoroborates with borylated aryl bromides via photoredox/nickel dual catalysis Protecting-group-free synthesis as an opportunity for invention Amphotericin primarily kills yeast by simply binding ergosterol A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates. 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 Total synthesis of synechoxanthin through iterative cross-coupling Synthesis of most polyene natural product motifs using just 12 building blocks and one coupling reaction A simple and general platform for generating stereochemically complex polyene frameworks by iterative cross-coupling Orthogonal reactivity in boryl-substituted organotrifluoroborates Modular synthesis of polyene side chain analogues of the potent macrolide antibiotic etnangien by a flexible coupling strategy based on hetero-bis-metallated alkenes General method for synthesis of 2-heterocyclic N-methyliminodiacetic acid boronates. Electrophilic C-H Borylation and Related Reactions of B-H Boron Cations Multistep synthesis of complex boronic acids from simple MIDA boronates The Pyridyldiisopropylsilyl Group: A Masked Functionality and Directing Group for Monoselective ortho-Acyloxylation and ortho-Halogenation Reactions of Arenes. A general strategy toward aromatic 1,2-ambiphilic synthons: palladium-catalyzed ortho-halogenation of PyDipSi-arenes Functionalized olefin cross-coupling to construct carbon-carbon bonds. Visible light-promoted metal-free C-H activation: diarylketone-catalyzed selective benzylic mono- and difluorination Ligand-accelerated cross-coupling of C(sp2)-H bonds with arylboron reagents Enantioselective, organocatalytic oxy-michael addition to gamma/delta-hydroxy-alpha,beta-enones: boronate-amine complexes as chiral hydroxide synthons Simple, efficient, and modular syntheses of polyene natural products via iterative cross-coupling Iterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis (Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis Stereoretentive Suzuki-Miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-peridinin Cross-electrophile coupling: principles of reactivity and selectivity Reversible click reactions with boronic acids to build supramolecular architectures in water (1-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis Facile synthesis of borofragments and their evaluation in activity-based protein profiling Oxidative geminal functionalization of organoboron compounds. (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenylbutane-2,3-diol: Valuable reagent in the asymmetric synthesis of organoboronates Enantiomerically Pure Cyclopropylamines from Cyclopropylboronic Esters A general solution for the 2-pyridyl problem. Iridium(I)-catalyzed C-H Borylation of α,β-Unsaturated Esters with Bis(pinacolato)diboron. From synthesis to function via iterative assembly of N-methyliminodiacetic acid boronate building blocks Ru-catalysed C-H arylation of indoles and pyrroles with boronic acids: scope and mechanistic studies A facile and convenient sequential homobimetallic catalytic approach towards β-methylstyrenes. A one-pot Stille cross-coupling/isomerization strategy. Iterative Assembly of Macrocyclic Lactones using Successive Ring Expansion Reactions Direct catalytic cross-coupling of alkenyllithium compounds. Chemoselective boronic ester synthesis by controlled speciation. Dynamic Core-Shell Bioconjugates for Targeted Protein Delivery and Release A Divalent Protecting Group for Benzoxaboroles The Molecular Industrial Revolution: Automated Synthesis of Small Molecules. A modular and concise approach to MIDA acylboronates via chemoselective oxidation of unsymmetrical geminal diborylalkanes: unlocking access to a novel class of acylborons An improved, scalable synthesis of Notum inhibitor LP-922056 using 1-chloro-1,2-benziodoxol-3-one as a superior electrophilic chlorinating agent Aryl derivatives of 3H-1,2-benzoxathiepine 2,2-dioxide as carbonic anhydrase inhibitors Near-IR BODIPY Dyes à la Carte-Programmed Orthogonal Functionalization of Rationally Designed Building Blocks. Oxidation of organotrifluoroborates via oxone A method for the deprotection of alkylpinacolyl boronate esters ortho-Selective nucleophilic addition of amines to 3-borylbenzynes: synthesis of multisubstituted anilines by the triple role of the boryl group. Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate Boryl (Hetero)aryne Precursors as Versatile Arylation Reagents: Synthesis through C-H Activation and Orthogonal Reactivity. Iterative protecting group-free cross-coupling leading to chiral multiply arylated structures. MIDA boronates are hydrolysed fast and slow by two different mechanisms. A general method for Suzuki-Miyaura coupling reactions using lithium triisopropyl borates

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