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NaH-mediated direct C–H arylation in the presence of 1,10-phenanthroline

Kanako Nozawa‐Kumada, Yuki Iwakawa, So Onuma, Masanori Shigeno, Yoshinori Kondo

2020Chemical Communications12 citationsDOI

Abstract

Transition-metal-free coupling of haloarenes with unactivated arenes has been developed in the presence of NaH and 1,10-phenanthroline. Various haloarenes bearing methyl, methoxy, halogen (fluoride, chloride, and bromide), cyano, trifluoromethyl, ester, and amide groups can be cross-coupled with unactivated arenes, or heteroarenes in this reaction.

Topics & Concepts

PhenanthrolineChemistryCombinatorial chemistryTransition metalPolymer chemistryMedicinal chemistryCatalysisOrganic chemistryCatalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsRadical Photochemical Reactions
NaH-mediated direct C–H arylation in the presence of 1,10-phenanthroline | Litcius