About: Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols

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About: Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols Goto Sponge NotDistinct Permalink

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scientific article published on 28 February 2008

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rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2008 (ast) наукова стаття, опублікована в лютому 2008 (uk) مقالة علمية نشرت في 28 فبراير 2008 (ar) scientific article published on 28 February 2008 (en)
publication date	wds:Q37400483-D6923CD7-004E-43B0-8BCF-30F6D8F59980
publication date	2008-02-28 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37400483-F111FCB9-B8BC-4A83-8239-93F2DA92B4FF
language of work or name	English
cites work	wds:Q37400483-066D3873-8708-4897-B357-4C2AE03910BA wds:Q37400483-0B5FBF4A-26E1-41EE-B49A-B03BBEA7BD4C wds:Q37400483-0D4F0CB2-1519-4560-8485-63844F5A8416 wds:Q37400483-15D6E512-5776-482C-9650-3256DE45535C wds:Q37400483-29B40C8C-289D-4AA2-9D36-A19BFB55650D wds:Q37400483-342E98EF-DCDD-49CA-999C-E796B52CE2A3 wds:Q37400483-35206202-7AA4-4EE7-AC0D-844F2B21AEB4 wds:Q37400483-41EAE200-9000-4B01-9B9B-8738774677A4 wds:Q37400483-4361CA6B-C8BD-4146-89AE-150DEC088877 wds:Q37400483-548DA18A-4281-47AA-B3F8-DA8C74A19BBA wds:Q37400483-5E8534D5-7FAC-49D3-92CB-8939E230E9B1 wds:Q37400483-6CDD6A29-8628-4C13-AEA4-94F2BBE3D76B wds:Q37400483-74DB0D4B-6F76-4593-BFAE-BD7A85E33ACB wds:Q37400483-7763514E-1E80-46D1-856A-767D329BE92B wds:Q37400483-7D1B80EF-A4B4-44D3-9D0D-DF6E70E43A32 wds:Q37400483-91A4CB10-5B2B-483E-B0EB-1C04070C0A4F wds:Q37400483-9AC21A2A-5B4E-467F-9478-2856687AC68B wds:Q37400483-AEE83CAA-8011-44E6-840F-4DDC663765EB wds:Q37400483-BCB4D629-B260-42F3-94D3-9CB791911B8A wds:Q37400483-BFEC4EA6-511C-4434-B04D-A1CEF441CDC8 wds:Q37400483-CA8BC38B-F519-4774-AF12-3940B05B182D wds:Q37400483-CCC5851A-2DF2-43D1-9EC9-660F2191F483 wds:Q37400483-CFFF1744-8F6D-43C3-A125-F47FD961E075 wds:Q37400483-D8109076-7D98-442E-9EC1-0C5E1AD19361 wds:Q37400483-E04A3C6B-6F0C-4A21-84E4-9819A692FC5F wds:Q37400483-ED209F2A-9B02-49EA-9EB2-A5755C33578F wds:Q37400483-F28D2879-3D52-4E6F-9716-7C060C2820B2 wds:Q37400483-F6343E96-C473-46FD-8ACA-DBB20FD65D0B
cites work	Suzuki cross-coupling reactions of potassium alkenyltrifluoroborates Catalysts for Suzuki-Miyaura coupling processes: scope and studies of the effect of ligand structure Palladium-Catalyzed Carboetherification and Carboamination Reactions of γ-Hydroxy- and γ-Aminoalkenes for the Synthesis of Tetrahydrofurans and Pyrrolidines Intramolecular silicon-assisted cross-coupling reactions: general synthesis of medium-sized rings containing a 1,3-cis-cis diene unit Intramolecular silicon-assisted cross-coupling: total synthesis of (+)-brasilenyne Tandem intramolecular silylformylation and silicon-assisted cross-coupling reactions. synthesis of geometrically defined alpha,beta-unsaturated aldehydes Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides Generation of substituted styrenes via Suzuki cross-coupling of aryl halides with 2,4,6-trivinylcyclotriboroxane Simple and efficient protocol for the synthesis of functionalized styrenes from 1,2-dibromoethane and arylboronic acids Heterodimerization of Olefins. 1. Hydrovinylation Reactions of Olefins That Are Amenable to Asymmetric Catalysis Fluoride-promoted cross-coupling reactions of alkenylsilanols. Elucidation of the mechanism through spectroscopic and kinetic analysis Sequential silylcarbocyclization/silicon-based cross-coupling reactions Advances in homogeneous and heterogeneous catalytic asymmetric epoxidation Sequential ring-closing metathesis and silicon-assisted cross-coupling reactions: stereocontrolled synthesis of highly substituted unsaturated alcohols Cross-coupling reactions of alkenylsilanolates. Investigation of the mechanism and identification of key intermediates through kinetic analysis Palladium-catalyzed aerobic oxidative amination of alkenes: development of intra- and intermolecular aza-Wacker reactions Regio- and enantiocontrol in the room-temperature hydroboration of vinyl arenes with pinacol borane Phosphine Oxides as Stabilizing Ligands for the Palladium-Catalyzed Cross-Coupling of Potassium Aryldimethylsilanolates Catalytic asymmetric hydroamination of non-activated olefins Suzuki-Miyaura cross-coupling reactions of potassium vinyltrifluoroborate with aryl and heteroaryl electrophiles Design and implementation of new, silicon-based, cross-coupling reactions: importance of silicon-oxygen bonds Palladium-catalyzed cross-coupling reactions of heterocyclic silanolates with substituted aryl iodides and bromides Palladium-catalyzed cross-coupling reactions of silanolates: a paradigm shift in silicon-based cross-coupling reactions Fluoride-free cross-coupling of organosilanols Mild and general cross-coupling of (alpha-Alkoxyvinyl)silanols and -silyl hydrides Vinylation of aryl bromides using an inexpensive vinylpolysiloxane Palladium/Imidazolium Salt Catalyzed Coupling of Aryl Halides with Hypervalent Organostannates Stereospecific palladium-catalyzed cross-coupling of (E)- and (Z)-alkenylsilanolates with aryl chlorides
author name string	wds:Q37400483-657DDC66-04E3-49DF-B843-A73ECBC3ED88 wds:Q37400483-7FCB93C0-F0F0-461F-AD62-5106C4B06609
author name string	Christopher R Butler Scott E Denmark
rdfs:label	Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (en) Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (nl) Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (ast)
skos:prefLabel	Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (en) Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (nl) Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (ast)
name	Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (en) Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (nl) Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (ast)
title	wds:Q37400483-F0BC2F76-28CE-46F2-A858-D5DB9B7E7DD8
title	Vinylation of aromatic halides using inexpensive organosilicon reagents. Illustration of design of experiment protocols (en)
page(s)	wds:Q37400483-3E207A46-1399-4678-B111-087637783431
page(s)	3690-3704
instance of	wds:Q37400483-0D23FF89-E7F6-4908-BAA8-47224DA0A0A8
instance of	scholarly article
PubMed ID	wds:Q37400483-8C2EAA53-DB4A-4808-8E11-3B7172E13D1D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18303892
PubMed ID	18303892
published in	wds:Q37400483-7C8C674E-0DE1-4DE3-8060-00F85231B215

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