Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design.
about
A synthetic, catalytic and theoretical investigation of an unsymmetrical SCN pincer palladacycleSynthesis of Hetero-bifunctional, End-Capped Oligo-EDOT Derivatives.Palladium-catalysed transannular C-H functionalization of alicyclic aminesBiaryl Phosphane Ligands in Palladium-Catalyzed AminationAuxiliary-assisted palladium-catalyzed arylation and alkylation of sp2 and sp3 carbon-hydrogen bonds.Pd0/PR3-catalyzed arylation of nicotinic and isonicotinic acid derivativesPalladium(II)-catalyzed ortho alkylation of benzoic acids with alkyl halidesAmide-Directed Arylation of sp C-H Bonds using Pd(II) and Pd(0) CatalystsCationic Pd(II)-catalyzed Fujiwara-Moritani reactions at room temperature in water.C-H bonds as ubiquitous functionality: a general approach to complex arylated pyrazoles via sequential regioselective C-arylation and N-alkylation enabled by SEM-group transposition.Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: departure from chirally modified allyl metal reagents in carbonyl additionCross-coupling of C(sp)-H Bonds with Organometallic Reagents via Pd(II)/Pd(0) Catalysis**Cobalt(III)-catalyzed synthesis of indazoles and furans by C-H bond functionalization/addition/cyclization cascades.Intramolecular arylation of benzimidazoles via Pd(II)/Cu(I) catalyzed cross-dehydrogenative coupling.Tuning reactivity and site selectivity of simple arenes in C-H activation: ortho-arylation of anisoles via arene-metal π-complexation.TADDOL-based phosphorus(III)-ligands in enantioselective Pd(0)-catalysed C-H functionalisations.C-H bonds as ubiquitous functionality: preparation of multiple regioisomers of arylated 1,2,4-triazoles via C-H arylation.Stapled Peptides by Late-Stage C(sp3 )-H Activation.Decarboxylative and dehydrative coupling of dienoic acids and pentadienyl alcohols to form 1,3,6,8-tetraenes.Dehydrogenative alkenylation of uracils via palladium-catalyzed regioselective C-H activation.Direct transition metal-catalyzed functionalization of heteroaromatic compoundsPd(II)-catalyzed olefination of electron-deficient arenes using 2,6-dialkylpyridine ligandsRh(I)-catalyzed arylation of heterocycles via C-H bond activation: expanded scope through mechanistic insight.Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bondsPalladium-Catalyzed C-H Arylation of 1,2,3-Triazoles.Synthesis of Fluorenes via the Palladium-Catalyzed 5-Exo-dig Annulation of o-Alkynyl Biaryls.Superelectrophilic intermediates in nitrogen-directed aromatic borylation.Catalytic Reductive ortho-C-H Silylation of Phenols with Traceless, Versatile Acetal Directing Groups and Synthetic Applications of DioxasilinesPalladium-Catalyzed, Site-Selective Direct Allylation of Aryl C-H Bonds by Silver-Mediated C-H Activation: A Synthetic and Mechanistic Investigation.Intermolecular oxidative cross-coupling of arenes.Organometallic aspects of transition-metal catalysed regioselective C-H bond functionalisation of arenes and heteroarenes.Arene C-H functionalisation using a removable/modifiable or a traceless directing group strategy.Carbon-Hydrogen (C-H) Bond Activation at Pd(IV): A Frontier in C-H Functionalization Catalysis.Modification of purine and pyrimidine nucleosides by direct C-H bond activation.Palladium-catalyzed dehydrogenation/oxidative cross-coupling sequence of β-heteroatom-substituted ketones.Cyclen-conjugated rhodamine hydroxamate as Pd(2+)-specific fluorescent chemosensor.Catalytic C-H bond functionalisation of purine and pyrimidine nucleosides: a synthetic and mechanistic perspective.Selective detection and bio-imaging of Pd2+ with novel 'C-CN' bond cleavage of cyano-rhodamine, cyanation with diaminomaleonitrile.A new rhodamine based colorimetric 'off-on' fluorescence sensor selective for Pd2+ along with the first bound X-ray crystal structure.
P2860
Q28603481-8CF93D6F-6E14-4144-86F1-6B29F161C981Q28818169-229A4A47-1F9C-4C3D-98F9-B179A7914E09Q28820908-C21AD09C-A06C-4C98-8850-AB1574F4DAEDQ29041849-600493C9-F80E-4BB3-8E53-E470A74A38E0Q33737426-6958446B-1EDE-4451-8750-4F50EB162A95Q33867816-2C12BA9B-9732-4C83-9AC8-1AF86DCB1C5EQ34056894-973E0485-AAA0-407B-B077-A532F35400F9Q34061734-7596DB29-77B1-4DD1-AEC5-4D73166BECB1Q34108251-8CD1B0A4-31BD-452D-87FD-4686D7167C5CQ34198198-8552A23F-56E2-4C86-917A-AEF20645C195Q34848081-7C88CF2E-3F22-40D2-A34F-4BBE8C0A2E95Q34914538-49E203BE-FBCB-44E8-92BB-80FC56271B24Q35005974-CF2A7D45-3A33-40BB-B1DE-840FB9C56CFBQ35157361-7A3C8337-F9AF-4184-BC5C-3948DB2241B6Q35233781-3BE1DABC-705D-4E3E-BD9E-4C12F82B7273Q35825220-CEAD5F31-5784-4B3C-8D93-7EB9D9ACC60FQ35988842-B69309B4-A5B5-4E9B-BB77-1B3F8EAE40C4Q36207585-A1223935-88A7-4518-9F08-226DE0EB1B3FQ36337451-84E02BF8-E9F6-4A18-B395-04B0EE9AD0B8Q36806370-4832E344-D73E-4220-874B-E99F2497D040Q36852312-75791B3C-3921-43B2-9EDC-8DF209C6F8EDQ37154137-80374766-98DD-4692-A51C-5410834AF1D8Q37218691-08A871B9-B5A3-41CF-B6BC-DBAD6CE53E03Q37294999-8A145650-CF8B-4210-8FF2-923100C7BB43Q37307778-48C416E5-C450-47D3-A5FB-7DF2E4983642Q37379365-E4A62BCD-7FBB-42A2-BC0E-F5674C13646FQ37384916-0C7C86C3-9B03-4FB3-9DB9-A09B9CA1B569Q37390486-6A1F1689-B8C5-4CF0-BB1D-FBAB21CDD787Q37406215-E2FCDA72-B8EE-44BC-8803-9B087A0DD005Q37510346-478F778E-EA6A-448D-8253-4E0549B71AF8Q37683477-3899F100-F4FD-443F-8FE2-A04F3F592592Q38178035-3E38D71A-9C3F-42CD-88C5-BDAA7A1E40B4Q38225214-B6F8178F-67FD-414A-B426-DEA81B9A9758Q38302114-736C56B1-2A2C-4046-8EDD-CB557DB7571AQ38383928-24A8B86E-73F2-4F76-8C72-9F1D37873181Q38457733-A5CAD51A-5990-4386-BF38-5FF9677F0730Q38474797-45898BC9-9AD7-4089-A04A-566F35002A8AQ38518916-A71EA8AC-46AF-4D3A-A10F-DB237A778E05Q38548185-81794347-EF4B-444D-B228-39E77063AD81Q38549895-CFE9DA4A-9E78-4503-B4CF-B4C6B2DD8217
P2860
Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design.
description
2006 nî lūn-bûn
@nan
2006 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Palladium-catalyzed benzene ar ...... ey element in catalyst design.
@en
Palladium-catalyzed benzene ar ...... ey element in catalyst design.
@nl
type
label
Palladium-catalyzed benzene ar ...... ey element in catalyst design.
@en
Palladium-catalyzed benzene ar ...... ey element in catalyst design.
@nl
prefLabel
Palladium-catalyzed benzene ar ...... ey element in catalyst design.
@en
Palladium-catalyzed benzene ar ...... ey element in catalyst design.
@nl
P356
P1476
Palladium-catalyzed benzene ar ...... ey element in catalyst design.
@en
P2093
Keith Fagnou
Marc Lafrance
P304
16496-16497
P356
10.1021/JA067144J
P407
P577
2006-12-01T00:00:00Z