about
SET-induced biaryl cross-coupling: an S(RN)1 reaction.Trace metal impurities in catalysis.To be or not to be metal-free: trends and advances in coupling chemistries.Direct arylation and heterogeneous catalysis; ever the twain shall meet.Part I: the development of the catalytic Wittig reaction.Mild copper-mediated direct oxidative cross-coupling of 1,3,4-oxadiazoles with polyfluoroarenes by using dioxygen as oxidant.Unexpectedly Simple Synthesis of Benzazoles by tBuONa-Catalyzed Direct Aerobic Oxidative Cyclocondensation of o-Thio/Hydroxy/Aminoanilines with Alcohols under Air.Aqueous synthesis of 1-H-2-substituted benzimidazoles via transition-metal-free intramolecular amination of aryl iodides.Transition metal-free direct C–H bond thiolation of 1,3,4-oxadiazoles and related heteroarenesMagnetic Nanoparticles-Supported Palladium: A Highly Efficient and Reusable Catalyst for the Suzuki, Sonogashira, and Heck ReactionsImmobilized Pd on magnetic nanoparticles bearing proline as a highly efficient and retrievable Suzuki–Miyaura catalyst in aqueous mediaUse of dimethyl carbonate as a solvent greatly enhances the biaryl coupling of aryl iodides and organoboron reagents without adding any transition metal catalystsDeconvoluting the Innocent vs. Non-innocent Behavior of -diethylphenylazothioformamide Ligands with Copper SourcesPotassium tert-butoxide mediated Heck-type cyclization/isomerization–benzofurans from organocatalytic radical cross-coupling reactions
P2860
Q37700989-1B1F0AC0-81D1-4233-BA4F-7F022B671786Q37973259-5326C7BD-6116-455B-A473-09B18F53678FQ38161784-691639A2-3069-4810-89D3-A56E5D3A4994Q38958646-BC2037A7-4894-4D66-8FE9-F45021EB7F4CQ43951980-D565046F-5D60-4102-B374-CB9D79110FA4Q45152068-47299B5D-CB8A-4456-A824-1C0F91A73837Q50269480-51615BC0-CE4A-4859-9759-4116D37C9837Q50488756-6769611D-60F3-42D9-ADC2-507768223DD7Q57404790-368E65E5-CC23-4E67-BFBE-58C8FA3AEEA4Q57614601-3210ED22-9B8B-48A5-BA0E-1277180E30EAQ57954144-9DD45B21-ABC3-403B-8622-5C177297FA2CQ58169581-BA0472F5-9CA4-49D0-BFDF-71B416C6EAA7Q58584608-9A90FFF8-63AE-4068-B9BB-D1CFE128A2AFQ59071610-ED6A9DF6-C3F3-4752-83BE-BFB2D4C8A4FB
P2860
description
2010 nî lūn-bûn
@nan
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
2010年论文
@zh
2010年论文
@zh-cn
name
Cross coupling: When is free really free?
@en
Cross coupling: When is free really free?
@nl
type
label
Cross coupling: When is free really free?
@en
Cross coupling: When is free really free?
@nl
prefLabel
Cross coupling: When is free really free?
@en
Cross coupling: When is free really free?
@nl
P356
P1433
P1476
Cross coupling: When is free really free?
@en
P2888
P304
P356
10.1038/NCHEM.913
P577
2010-11-07T00:00:00Z
P6179
1030093921