In recent years, the cross-dehydrogenative coupling (CDC) has demonstrated to be a powerful synthetic tool to form C–C bonds from two C–H bonds. This high atom-economic transformation is an attractive alternative to the classical substitution and coupling approaches for the benzylation and allylation of carbon centers, which rely on the reaction of adequately functionalized starting materials. This review emphasizes the utility of the CDC through the coupling of benzylic and allylic C–H bonds with C(sp)–H, C(sp2)–H and C(sp3)–H bonds.This work was generously supported by the Spanish Ministerio de Ciencia, Innovación y Universidades (MICIU; grant no. CTQ2017-88171-P), the Generalitat Valenciana (GV; grant no. AICO/2017/007) and the Universid...
International audienceRecent years have witnessed tremendous improvement in the development of effic...
International audienceRecent years have witnessed tremendous improvement in the development of effic...
The use of cross-coupling reactions for the preparation of alkylated and arylated heteroaromatic com...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
The synthesis of biologically active small molecules is crucial for drug discovery and treatment of ...
Cross-dehydrogenative coupling (CDC) is a process in which, typically, a C–C bond is formed at the e...
Cross-dehydrogenative coupling (CDC) is a process in which, typically, a C–C bond is formed at the e...
The direct formation of C-C/C-X bonds from unfunctionalized C-H/X-H bonds is termed as cross-dehydro...
The direct formation of C-C/C-X bonds from unfunctionalized C-H/X-H bonds is termed as cross-dehydro...
The direct formation of C-C/C-X bonds from unfunctionalized C-H/X-H bonds is termed as cross-dehydro...
Formation of all-carbon-substituted quaternary carbons is a key challenge in organic and medicinal c...
The functionalization of carbon-hydrogen bonds in non-nucleophilic substrates using α-carbonyl sulfo...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
The functionalization of typically unreactive C(sp3)–H bondsholds great promise for reducing th...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
International audienceRecent years have witnessed tremendous improvement in the development of effic...
International audienceRecent years have witnessed tremendous improvement in the development of effic...
The use of cross-coupling reactions for the preparation of alkylated and arylated heteroaromatic com...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
The synthesis of biologically active small molecules is crucial for drug discovery and treatment of ...
Cross-dehydrogenative coupling (CDC) is a process in which, typically, a C–C bond is formed at the e...
Cross-dehydrogenative coupling (CDC) is a process in which, typically, a C–C bond is formed at the e...
The direct formation of C-C/C-X bonds from unfunctionalized C-H/X-H bonds is termed as cross-dehydro...
The direct formation of C-C/C-X bonds from unfunctionalized C-H/X-H bonds is termed as cross-dehydro...
The direct formation of C-C/C-X bonds from unfunctionalized C-H/X-H bonds is termed as cross-dehydro...
Formation of all-carbon-substituted quaternary carbons is a key challenge in organic and medicinal c...
The functionalization of carbon-hydrogen bonds in non-nucleophilic substrates using α-carbonyl sulfo...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
The functionalization of typically unreactive C(sp3)–H bondsholds great promise for reducing th...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
International audienceRecent years have witnessed tremendous improvement in the development of effic...
International audienceRecent years have witnessed tremendous improvement in the development of effic...
The use of cross-coupling reactions for the preparation of alkylated and arylated heteroaromatic com...