A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
about
Asymmetric intermolecular boron Heck-type reactions via oxidative palladium(II) catalysis with chiral tridentate NHC-amidate-alkoxide ligandsPalladium-catalyzed oxidative intermolecular difunctionalization of terminal alkenes with organostannanes and molecular oxygenPd(II)-catalyzed oxidative 1,1-diarylation of terminal olefins.A highly selective and general palladium catalyst for the oxidative Heck reaction of electronically nonbiased olefins.Operationally simple and highly (E)-styrenyl-selective Heck reactions of electronically nonbiased olefins.Development of Stereocontrolled Palladium(II)-Catalyzed Domino Heck/Suzuki β,α-Diarylation Reactions with Chelating Vinyl Ethers and Arylboronic Acids.Imparting catalyst control upon classical palladium-catalyzed alkenyl C-H bond functionalization reactionsCatalyst-controlled regioselectivity in the synthesis of branched conjugated dienes via aerobic oxidative Heck reactions.Enantioselective redox-relay oxidative heck arylations of acyclic alkenyl alcohols using boronic acids.Palladium(II)-catalyzed Heck reaction of aryl halides and arylboronic acids with olefins under mild conditions.A new approach to carbon-carbon bond formation: Development of aerobic Pd-catalyzed reductive coupling reactions of organometallic reagents and styrenes.Palladium-Catalyzed 1,3-Difunctionalization Using Terminal Alkenes with Alkenyl Nonaflates and Aryl Boronic AcidsMechanism, reactivity, and selectivity in palladium-catalyzed redox-relay Heck arylations of alkenyl alcohols.The emergence of sulfoxides as efficient ligands in transition metal catalysis.Enantioselective oxidative boron Heck reactions.C-H Coupling Reactions Directed by Sulfoxides: Teaching an Old Functional Group New Tricks.Aerobic oxidative Heck/dehydrogenation reactions of cyclohexenones: efficient access to meta-substituted phenols.Recent advancements and challenges of palladium(II)-catalyzed oxidation reactions with molecular oxygen as the sole oxidant.Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reactionIterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis.Allylic C-H amination for the preparation of syn-1,3-amino alcohol motifs.Regioselective aerobic oxidative Heck reactions with electronically unbiased alkenes: efficient access to α-alkyl vinylarenes.Aqueous oxidative Heck reaction as a protein-labeling strategy.Alternative pathways for Heck intermediates: palladium-catalyzed oxyarylation of homoallylic alcoholsOxidative Heck vinylation for the synthesis of complex dienes and polyenes.Sequential allylic C-H amination/vinylic C-H arylation: a strategy for unnatural amino acid synthesis from α-olefins.Pd(II)-catalyzed highly selective arylation of allyl esters via C-H functionalization of unreactive arenes with retention of the traditional leaving group.Scalable synthesis of oxazolones from propargylic alcohols through multistep palladium(II) catalysis: β-selective oxidative Heck coupling of cyclic sulfonyl enamides and aryl boroxines.Dynamic Strategic Bond Analysis Yields a Ten-Step Synthesis of 20-nor-Salvinorin A, a Potent κ-OR Agonist.Conjugated Microporous Polymers for Heterogeneous Catalysis.Catalytic Oxidative Trifluoromethoxylation of Allylic C-H Bonds Using a Palladium Catalyst.Auto-Tandem Catalysis: PdII -Catalysed Dehydrogenation/Oxidative Heck Reaction of Cyclopentane-1,3-diones.Palladium-catalyzed cross-coupling of unactivated alkenes with acrylates: application to the synthesis of the C13-C21 fragment of palmerolide A.Intermolecular Mizoroki-Heck reaction of aliphatic olefins with high selectivity for substitution at the internal position.Stereoselective synthesis of highly substituted enamides by an oxidative Heck reaction.Diastereoselective sp2-sp3 coupling of sugar enol ethers with unactivated cycloalkenes: new entries to C-branched sugars.3-Acylindoles via palladium-catalyzed regioselective arylation of electron-rich olefins with indoles
P2860
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P2860
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
@en
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
@nl
type
label
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
@en
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
@nl
prefLabel
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
@en
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
@nl
P2093
P356
P1476
A general and highly selective chelate-controlled intermolecular oxidative Heck reaction.
@en
P2093
Alexandria P Brucks
Jared H Delcamp
M Christina White
P304
11270-11271
P356
10.1021/JA804120R
P407
P577
2008-07-31T00:00:00Z