An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides
about
sameAs
DualPhos: a versatile, chemoselective reagent for two-carbon aldehyde to latent (E)-alkenal homologation and application in the total synthesis of phomolide GCinnamaldehyde Derivatives Inhibit Coxsackievirus B3-Induced Viral MyocarditisStructure-activity relationship of cinnamaldehyde analogs as inhibitors of AI-2 based quorum sensing and their effect on virulence of Vibrio sppA general organocatalyzed Michael-Michael cascade reaction generates functionalized cyclohexenes.Mechanism, reactivity, and selectivity in palladium-catalyzed redox-relay Heck arylations of alkenyl alcohols.Synthesis of functionalized cinnamaldehyde derivatives by an oxidative Heck reaction and their use as starting materials for preparation of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase inhibitors.Development of Hierarchical Polymer@Pd Nanowire-Network: Synthesis and Application as Highly Active Recyclable Catalyst and Printable Conductive InkEthylenation of aldehydes to 3-propanal, propanol and propanoic acid derivatives.Alpha'-hydroxyenones as mechanistic probes and scope-expanding surrogates for alpha,beta-unsaturated aldehydes in N-heterocyclic carbene-catalyzed reactions.Pd-catalyzed cascade Heck-Saegusa: direct synthesis of enals from aryl iodides and allyl alcohol.Organocatalytic regiospecific synthesis of 1H-indene-2-carbaldehyde derivatives: suppression of cycloolefin isomerisation by employing sterically demanding catalysts.Organocatalyzed Asymmetric Conjugate Addition of Heteroaryl and Aryl Trifluoroborates: a Synthetic Strategy for Discoipyrrole D.Domino-hydroformylation/aldol condensation catalysis: highly selective synthesis of α,β-unsaturated aldehydes from olefins.Copper-catalyzed formylation of alkenyl C-H bonds using BrCHCl2 as a stoichiometric formylating reagent.
P2860
Q28585018-FB26663F-278F-4A9C-8839-6FCEC6AEC559Q33655891-76FDB398-F109-473C-9063-9B8C3124FC48Q33797898-20622F57-2F2B-49AC-9A95-BB4620E6032FQ35414251-6F4F1928-1DEF-470B-8133-AA73D3AA0487Q37701627-F0925EBC-866E-40DE-B265-9663B1F043D7Q38856166-C836A649-51C7-4DAF-AFBA-F44DB2EAE26CQ42062782-91B1C22D-0EC8-4939-89FD-9B1C930C461EQ42117341-804B0C4F-CFB6-4BC8-8DE6-5BDA5F8FDBEAQ42208767-A8716005-7658-45E0-AC64-940D906B4075Q43196945-984DD03A-B63E-48A0-8DC8-8D693C0BF176Q48053149-925F5B27-B8DD-4738-98DC-70F9D6024EB8Q50963584-5188B2A6-521E-427D-9632-BA8DE41D6419Q52778337-64C0EF29-C85A-40F4-AF10-84EE158E7A70Q55410238-3B330655-5518-4CC9-9016-6D2F127554B8
P2860
An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
An efficient palladium-catalyz ...... and aryl iodides and bromides
@ast
An efficient palladium-catalyz ...... and aryl iodides and bromides
@en
An efficient palladium-catalyz ...... and aryl iodides and bromides
@nl
type
label
An efficient palladium-catalyz ...... and aryl iodides and bromides
@ast
An efficient palladium-catalyz ...... and aryl iodides and bromides
@en
An efficient palladium-catalyz ...... and aryl iodides and bromides
@nl
prefLabel
An efficient palladium-catalyz ...... and aryl iodides and bromides
@ast
An efficient palladium-catalyz ...... and aryl iodides and bromides
@en
An efficient palladium-catalyz ...... and aryl iodides and bromides
@nl
P2093
P356
P1433
P1476
An efficient palladium-catalyz ...... and aryl iodides and bromides
@en
P2093
Giancarlo Fabrizi
Gianfranco Battistuzzi
Sandro Cacchi
P304
P356
10.1021/OL034071P
P407
P577
2003-03-06T00:00:00Z