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Enantioselective construction of remote quaternary stereocentresPalladium-Catalyzed Enantioselective Heck Alkenylation of Trisubstituted Allylic Alkenols: A Redox-Relay Strategy to Construct Vicinal StereocentersEnantioselective and Enantiospecific Transition-Metal-Catalyzed Cross-Coupling Reactions of Organometallic Reagents To Construct C-C BondsAdaptable P-X Biaryl Phosphite/Phosphoroamidite-Containing Ligands for Asymmetric Hydrogenation and C-X Bond-Forming Reactions: Ligand Libraries with Exceptionally Wide Substrate Scope.Relative reactivity of alkenyl alcohols in the palladium-catalyzed redox-relay Heck reaction.Catalyst-controlled regioselectivity in the synthesis of branched conjugated dienes via aerobic oxidative Heck reactions.Alkenyl carbonyl derivatives in enantioselective redox relay Heck reactions: accessing α,β-unsaturated systemsPalladium-catalyzed enantioselective Heck alkenylation of acyclic alkenols using a redox-relay strategy.Enantioselective redox-relay oxidative heck arylations of acyclic alkenyl alcohols using boronic acids.Enantioselective Dehydrogenative Heck Arylations of Trisubstituted Alkenes with Indoles to Construct Quaternary StereocentersEnantioselective Palladium-Catalyzed Alkenylation of Trisubstituted Alkenols To Form Allylic Quaternary Centers.Catalytic enantioselective cyclization/cross-coupling with alkyl electrophiles.Mechanism, reactivity, and selectivity in palladium-catalyzed redox-relay Heck arylations of alkenyl alcohols.To be or not to be metal-free: trends and advances in coupling chemistries.Fluorometric imaging methods for palladium and platinum and the use of palladium for imaging biomolecules.Enantioselective oxidative boron Heck reactions.Regioselective synthesis of naphthoquinone/naphthoquinol-carbohydrate hybrids by [4 + 2] anionic annulations and studies on their cytotoxicity.1,1-Disubstituted olefin synthesis via Ni-catalyzed Markovnikov hydroalkylation of alkynes with alkyl halides.Enantioselective assembly of tertiary stereocenters via multicomponent chemoselective cross-coupling of geminal chloro(iodo)alkanes.Palladium-Catalyzed Enantioselective Redox-Relay Heck Alkynylation of Alkenols To Access Propargylic Stereocenters.An effective Pd nanocatalyst in aqueous media: stilbene synthesis by Mizoroki-Heck coupling reaction under microwave irradiation.Enantioselective Narasaka-Heck cyclizations: synthesis of tetrasubstituted nitrogen-bearing stereocentersAsymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.Enantioselective Heck arylations of acyclic alkenyl alcohols using a redox-relay strategy.Palladium-catalyzed asymmetric intermolecular cyclization.Facile access to cis-2,6-disubstituted tetrahydropyrans by palladium-catalyzed decarboxylative allylation: total syntheses of (±)-centrolobine and (+)-decytospolides A and B.Scalable synthesis of oxazolones from propargylic alcohols through multistep palladium(II) catalysis: β-selective oxidative Heck coupling of cyclic sulfonyl enamides and aryl boroxines.Achieving vinylic selectivity in Mizoroki-Heck reaction of cyclic olefins.Mizoroki-Heck Cyclizations of Amide Derivatives for the Introduction of Quaternary Centers.Access to enantioenriched 2,3- and 2,5-dihydrofurans with a fully substituted C2 stereocenter by Pd-catalyzed asymmetric intermolecular Heck reaction.Asymmetric Intermolecular Heck Reaction of Propargylic Acetates and Cycloalkenes to Access Fused Cyclobutenes.Nickel-Catalyzed Asymmetric Reductive Heck Cyclization of Aryl Halides to Afford Indolines.Palladium-Catalyzed Enantioselective Narasaka-Heck Reaction/Direct C-H Alkylation of Arenes: Iminoarylation of Alkenes.Heteromultimetallic catalysis for sustainable organic syntheses.Unlocking Mizoroki-Heck-Type Reactions of Aryl Cyanides Using Transfer Hydrocyanation as a Turnover-Enabling Step.Enantioselective total synthesis of the highly selective sphingosine-1-receptor VPC01091 by the Heck desymmetrization of a non-activated cyclopentene-fused spiro-pyrrolidinone.Enantioselective Formal C(sp2 )-H Vinylation.Artificial Force Induced Reaction Method for Systematic Determination of Complex Reaction Mechanisms.Enantioselective Synthesis of Chromenes via a Palladium-Catalyzed Asymmetric Redox-Relay Heck Reaction.Heck-like Reactions Involving Heteroatomic Electrophiles.
P2860
Q33554259-E196817C-E7AC-4E87-911A-6F80214C0AA0Q33574701-9D4C034F-BF1C-4193-89A0-05CC5C7F4655Q36049587-A36F1589-FA53-4EA8-A14A-6C6781F5F7EAQ36057224-5F32F0AE-15F6-4F4E-9921-9E140995E733Q36069302-B6E019A1-0CAE-4D84-BE7A-1DB8E4EF1568Q36392607-E9334C7F-609E-45D6-9759-4F93B74DEEC6Q36671943-5B181F29-DB57-474A-8555-A2140024F66FQ36671969-464179BF-CAE9-444B-A5D5-BFD08D1D2668Q36974478-7A8EB8BF-4C76-45F0-BEDE-9D1C7AA22C5CQ37289750-2956D359-DA4E-40F2-9DC0-6E59FB633B6AQ37494897-49A58CF6-B685-428D-B0AC-1A4E63303D84Q37701007-CC1C4B0C-BCCE-4BA5-AA5A-8570C4AAE429Q37701627-5797A9C9-0CAD-4DA0-9F35-754E0D411FFBQ38161784-621B8B8D-A3C2-4F66-A33A-E3E37B0923B5Q38364149-9F6D586D-4B01-41C4-8282-96F99E734B32Q38623384-27F071EB-42F8-4B30-A529-392DE6E730CFQ38736749-8B00B30A-4C2D-4C8D-9A4B-7C4FAFBC9742Q40361270-EDB47877-A9F7-402C-85E4-B2DCE942C1BEQ41092159-8AE8E6F2-1F93-46C9-BF76-6EF49763D962Q41136755-F7D5F987-609B-4D4C-A707-00A1692DC9A5Q41469091-8F108501-D59E-4E06-8EAA-9877366F7FB9Q41786209-E9108EE7-3AEE-4CF9-B4CF-7F79A11DCFD4Q42554304-589510B5-C942-4366-BAF8-EF62890AE821Q43238976-0F8C3B51-65D6-408C-A0A5-9B598701093EQ43730612-9481D10A-18B3-4E26-87E3-352876BDF537Q44902741-F25618F8-ACE5-4332-B81A-2290BAB2D6B0Q45898409-6655F48E-2B9C-4629-A360-7400BE5A0EEFQ46387018-619A5BD1-7257-4CE9-8B36-5C52F2149FB3Q46742612-D8A92652-41D0-4896-9C8C-EE2D44458C7CQ46849403-7B6D27C1-2169-40B6-977D-BB7DF94DB8FFQ47667399-96930182-8934-4F65-BFCE-A37E676A0876Q47727366-FFDFA417-A143-466F-A826-02E3F218AD52Q48011897-152EBCE7-84D8-4D50-A72E-A46C0A148443Q48051193-2AC53F70-ECC8-4069-8897-850BEC889FF6Q48293321-6EC37F33-5C97-4A55-B2DE-49AD2939A220Q48310639-263ACD7B-E55E-49DE-A822-A118417F0885Q48366542-9D9BC75C-5DE2-4B61-A442-06C46ADA84D3Q48972854-2748168E-2D74-49D7-BFAC-7F03B4DB462FQ49892367-3C783DA7-0A87-4D03-8F78-337B7A6AA927Q50147277-DC3C9B1E-FE1F-4271-ABF4-31B7F83FC274
P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
The asymmetric Heck and related reactions.
@ast
The asymmetric Heck and related reactions.
@en
The asymmetric Heck and related reactions.
@nl
type
label
The asymmetric Heck and related reactions.
@ast
The asymmetric Heck and related reactions.
@en
The asymmetric Heck and related reactions.
@nl
prefLabel
The asymmetric Heck and related reactions.
@ast
The asymmetric Heck and related reactions.
@en
The asymmetric Heck and related reactions.
@nl
P2860
P356
P1476
The asymmetric Heck and related reactions.
@en
P2093
Dennis Mc Cartney
Patrick J Guiry
P2860
P304
P356
10.1039/C1CS15101K
P577
2011-06-15T00:00:00Z