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ChemInform 2008, 39, issue 48 ©WlLEY-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Alkenes Q 0083 Nickel-Catalyzed Cross-Coupling Reaction of Allyl- and Benzylzinc with Alkenyl Sulfides. — To achieve good yields of target compounds (III), butyllithium must be added to form the Ni(0) catalyst. Coupling with zinc reagent (IV) results in formation of a mixture of regioisomers. For arylmethylzinc bromides, NiCl2(dppe) is the most effective catalyst. — (BABA, Y.; TOSHIMITSU, A.; MATSUBARA*, S.; Synlett 2008, 13, 2061-2063; Dep. Mater. Chem., Grad. Sch. Eng., Kyoto Univ., Nishikyo, Kyoto 615, Japan; Eng.) — S. Adam 48- 058

ChemInform Abstract: Nickel-Catalyzed Cross-Coupling Reaction of Allyl- and Benzylzinc with Alkenyl Sulfides

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AlkenesQ 0083 Nickel-Catalyzed Cross-Coupling Reaction of Allyl- and Benzylzinc with Alkenyl

Sulfides. — To achieve good yields of target compounds (III), butyllithium must be added to form the Ni(0) catalyst. Coupling with zinc reagent (IV) results in formation of a mixture of regioisomers. For arylmethylzinc bromides, NiCl2(dppe) is the most effective catalyst. — (BABA, Y.; TOSHIMITSU, A.; MATSUBARA*, S.; Synlett 2008, 13, 2061-2063; Dep. Mater. Chem., Grad. Sch. Eng., Kyoto Univ., Nishikyo, Kyoto 615, Japan; Eng.) — S. Adam

48- 058

ChemInform 2008, 39, issue 48 ©WlLEY-VCH Verlag GmbH & Co. KGaA, Weinheim