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• W1966965731 abstract "Asymmetric cross-coupling of dinaphtho[2,1-b:1',2'-d]thiophene with ArMgBr (Ar = Ph, 4-MeC6H4, 4-MeOC6H4) proceeded with high enantioselectivity in THF at 20 degrees C in the presence of 3 mol % of a nickel catalyst generated from Ni(cod)2 and a chiral oxazoline-phosphine ligand to give high yields of axially chiral 2-mercapto-2'-aryl-1,1'-binaphthyls, whose enantiomeric excesses are over 93%. The mercapto group in the chiral binaphthyl was converted into iodo, boryl, and phosphino groups without racemization." @default.
• W1966965731 created "2016-06-24" @default.
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• W1966965731 date "2002-10-17" @default.
• W1966965731 modified "2023-10-01" @default.
• W1966965731 title "Nickel-Catalyzed Asymmetric Grignard Cross-Coupling of Dinaphthothiophene Giving Axially Chiral 1,1‘-Binaphthyls" @default.
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• W1966965731 doi "https://doi.org/10.1021/ja0282588" @default.
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