A highly selective and general palladium catalyst for the oxidative Heck reaction of electronically nonbiased olefins.
about
Enantioselective construction of remote quaternary stereocentresOperationally simple and highly (E)-styrenyl-selective Heck reactions of electronically nonbiased olefins.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.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.Boron-Heck reaction of cyclic enaminones: regioselective direct arylation via oxidative palladium(II) catalysis.Catalytic selective synthesis.Enantioselective oxidative boron Heck reactions.Morphology dependent catalysis and surface enhanced Raman scattering (SERS) studies using Pd nanostructures in DNA, CTAB and PVA scaffolds.Aerobic oxidative Heck/dehydrogenation reactions of cyclohexenones: efficient access to meta-substituted phenols.Enantioselective Heck-Matsuda Arylations through Chiral Anion Phase-Transfer of Aryl Diazonium Salts.Palladium-Catalyzed Enantioselective Redox-Relay Heck Arylation of 1,1-Disubstituted Homoallylic Alcohols.Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles.Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reactionRegioselective aerobic oxidative Heck reactions with electronically unbiased alkenes: efficient access to α-alkyl vinylarenes.Aqueous oxidative Heck reaction as a protein-labeling strategy.Sequential allylic C-H amination/vinylic C-H arylation: a strategy for unnatural amino acid synthesis from α-olefins.Palladium-catalyzed regio- and stereoselective γ-arylation of tertiary allylic amines: identification of potent adenylyl cyclase inhibitors.Enantioselective Heck arylations of acyclic alkenyl alcohols using a redox-relay strategy.Scalable synthesis of oxazolones from propargylic alcohols through multistep palladium(II) catalysis: β-selective oxidative Heck coupling of cyclic sulfonyl enamides and aryl boroxines.Auto-Tandem Catalysis: PdII -Catalysed Dehydrogenation/Oxidative Heck Reaction of Cyclopentane-1,3-diones.DFT studies on the directing group dependent arene-alkene cross-couplings: arene activation vs. alkene activation.Oxidative Mizoroki-Heck-type reaction of arylsulfonyl hydrazides for a highly regio- and stereoselective synthesis of polysubstituted alkenes.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.A versatile approach to flavones via a one-pot Pd(II)-catalyzed dehydrogenation/oxidative boron-Heck coupling sequence of chromanones.
P2860
Q33554259-1D648FB3-B833-4DED-93F2-AFF97E1DDCACQ35070577-5C096C56-9EA2-49B5-ADC1-B9C505AF63B8Q35884164-EA99C014-17B3-45AE-B205-D26725253439Q36392607-07BF22EE-034B-4512-B06B-23013AECF775Q36974478-111F7EC3-C7E9-416B-8C79-28B969B5A84FQ37087967-F061D0DC-9300-4444-AEE2-2B379BEE28B4Q37316120-8E228C93-7730-42D4-BCEF-48839016C4ACQ37701627-32E702E8-BCEA-4ED1-9EC2-854A44B5237AQ37714049-702C2ECC-7D7D-49CC-9C16-92D102A8EB6FQ38046517-ABCC20BA-FECD-4D65-B156-5A48DEDDD58AQ38623384-CC42D0B8-2127-4075-AC8B-DF1D071063D7Q38656707-AC6E666C-CADF-4399-810B-39153B32278CQ40063349-E212AB88-103B-467D-99F7-E0427890606DQ41136749-161CA1C1-FAFF-43D6-84DF-63C734BBF339Q41198924-A5570069-1FF4-47E0-A83B-0BBB3C020C9BQ41671010-4F117388-6AE0-4039-A126-D3A880AF82C9Q41889268-B01B9115-51EA-471F-B745-8028BF7F85F2Q42128736-908A23F9-EBE7-43E0-A2B2-4DBDD82BE3F1Q42142287-C20406D7-6AB5-45C2-99E7-DA192664818DQ42741143-547D9B1E-6605-47AB-8EF8-7693CC60A33EQ43115360-5F660ABB-E3FB-4F54-AE9C-66471BBC98BFQ43238976-8403407F-1892-4480-804D-3DC494362371Q45898409-AE6C5796-EEE4-482B-BC02-0B303F6FBC0EQ48360378-F91B5BDA-AABE-4DFF-98D6-8EA144978810Q50264957-26050D72-34E9-48B0-999D-7554FCC7B7EDQ50504251-43C2BE69-F8F2-46B9-AAFA-E83A0266D4D9Q51371956-80C452FE-1586-4982-8438-FDB183D02DBFQ51553144-6DBFB192-B417-462D-BC71-9D3B2127A608Q53654927-58EB6705-2DA5-4C16-87AC-12AB31646F2C
P2860
A highly selective and general palladium catalyst for the oxidative Heck reaction of electronically nonbiased olefins.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
A highly selective and general ...... ctronically nonbiased olefins.
@ast
A highly selective and general ...... ctronically nonbiased olefins.
@en
A highly selective and general ...... ctronically nonbiased olefins.
@nl
type
label
A highly selective and general ...... ctronically nonbiased olefins.
@ast
A highly selective and general ...... ctronically nonbiased olefins.
@en
A highly selective and general ...... ctronically nonbiased olefins.
@nl
prefLabel
A highly selective and general ...... ctronically nonbiased olefins.
@ast
A highly selective and general ...... ctronically nonbiased olefins.
@en
A highly selective and general ...... ctronically nonbiased olefins.
@nl
P2860
P356
P1476
A highly selective and general ...... ctronically nonbiased olefins.
@en
P2093
Erik W Werner
Matthew S Sigman
P2860
P304
13981-13983
P356
10.1021/JA1060998
P407
P577
2010-10-01T00:00:00Z