365448-17-5Relevant articles and documents
Preparation of Polyfunctional Naphthyridines by Cobalt-Catalyzed Cross-Couplings of Halogenated Naphthyridines with Magnesium and Zinc Organometallics
Greiner, Robert,Ziegler, Dorothée S.,Cibu, Denise,Jakowetz, Andreas C.,Auras, Florian,Bein, Thomas,Knochel, Paul
, p. 6384 - 6387 (2017)
CoCl2 (5%) catalyzes cross-couplings of various halogenated naphthyridines with alkyl- and arylmagnesium halides. Also, arylzinc halides undergo smooth cross-couplings with various naphthyridines in the presence of CoCl2·2LiCl (5%) a
Ligand-Free Copper-Catalyzed Negishi Coupling of Alkyl-, Aryl-, and Alkynylzinc Reagents with Heteroaryl Iodides
Thapa, Surendra,Kafle, Arjun,Gurung, Santosh K.,Montoya, Adam,Riedel, Patrick,Giri, Ramesh
supporting information, p. 8236 - 8240 (2015/07/07)
Reported herein is an unprecedented ligand-free copper-catalyzed cross-coupling of alkyl-, aryl-, and alkynylzinc reagents with heteroaryl iodides. The reaction proceeds at room temperature for the coupling of primary, secondary, and tertiary alkylzinc reagents with heteroaryl iodides without rearrangement. An elevated temperature (100 C) is required for aryl-heteroaryl and alkynyl-heteroaryl couplings.