[[abstract]]A general synthesis of symmetrical biaryls in good to excellent yields via homo-coupling of aryl Grignard reagents in the presence of 2,3- dichloropropene is described.[[fileno]]2050103010019[[department]]生科
Cross-coupling reactions of Grignard reagents with functionalized aryl, heteroaryl, and sterically h...
Cross-coupling reactions of Grignard reagents with functionalized aryl, heteroaryl, and sterically h...
Highly selective C(sp2)–C(sp2) cross-coupling of dihalogenated hydrocarbons comprising C(sp2)–Br and...
Formation of biaryls occurs in reasonable yields under convenient conditions for both aryllithium re...
A one-step synthesis of symmetrical biaryls was developed and uses a nickel(III) complex containing ...
A one-step synthesis of symmetrical biaryls was developed and uses a nickel(III) complex containing ...
[[abstract]]A series of biaryls and biheteroaryls were synthesized by the Barbier reaction of aryl b...
The new well-defined catalyst [Pd(mu-Cl)Cl(IPr*)](2) enables the efficient Grignard reagent cross-co...
actions of functionalized alkenyl halides and a variety of Grignard reagents, including those bearin...
The nickel or palladium catalyzed cross-coupling reac-tions of organic halides or triflates with alk...
Reductive homocoupling of aryl halides in the presence of commercial zinc dust and ammonium formate ...
1137-1143A facile synthesis of biaryl systems has been achieved involving three-component coupling r...
It is over 100 years since scientists first postulated the existence of arynes as reactive intermedi...
1 - ArticleAryl Grignard reagents react stereospecifically with alkenyl halides in the presence of m...
publisher[Abstract] Under palladium catalysis, α-haloketones, such as chloroacetone or phenacyl chlo...
Cross-coupling reactions of Grignard reagents with functionalized aryl, heteroaryl, and sterically h...
Cross-coupling reactions of Grignard reagents with functionalized aryl, heteroaryl, and sterically h...
Highly selective C(sp2)–C(sp2) cross-coupling of dihalogenated hydrocarbons comprising C(sp2)–Br and...
Formation of biaryls occurs in reasonable yields under convenient conditions for both aryllithium re...
A one-step synthesis of symmetrical biaryls was developed and uses a nickel(III) complex containing ...
A one-step synthesis of symmetrical biaryls was developed and uses a nickel(III) complex containing ...
[[abstract]]A series of biaryls and biheteroaryls were synthesized by the Barbier reaction of aryl b...
The new well-defined catalyst [Pd(mu-Cl)Cl(IPr*)](2) enables the efficient Grignard reagent cross-co...
actions of functionalized alkenyl halides and a variety of Grignard reagents, including those bearin...
The nickel or palladium catalyzed cross-coupling reac-tions of organic halides or triflates with alk...
Reductive homocoupling of aryl halides in the presence of commercial zinc dust and ammonium formate ...
1137-1143A facile synthesis of biaryl systems has been achieved involving three-component coupling r...
It is over 100 years since scientists first postulated the existence of arynes as reactive intermedi...
1 - ArticleAryl Grignard reagents react stereospecifically with alkenyl halides in the presence of m...
publisher[Abstract] Under palladium catalysis, α-haloketones, such as chloroacetone or phenacyl chlo...
Cross-coupling reactions of Grignard reagents with functionalized aryl, heteroaryl, and sterically h...
Cross-coupling reactions of Grignard reagents with functionalized aryl, heteroaryl, and sterically h...
Highly selective C(sp2)–C(sp2) cross-coupling of dihalogenated hydrocarbons comprising C(sp2)–Br and...
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