Cross-dehydrogenative coupling (CDC) is a process in which, typically, a C–C bond is formed at the expense of two C–H bonds, either catalyzed by metals or other organic compounds, or via uncatalyzed processes. In this perspective, we present various modes of C–H bond-activation at sp3 centers adjacent to ether oxygen atoms, followed by C–C bond formation with aromatic systems as well as with heteroaromatic systems. C–N bond-formation with NH-containing heteroaromatics, leading to hemiaminal ethers, is also an event that can occur analogously to C–C bond formation, but at the expense of C–H and N–H bonds. A large variety of hemiaminal ether-forming reactions have recently appeared in the literature and this perspective also includes this com...
Catalytic oxidative cross-dehydrogenative coupling between unactivated C(sp<sup>2</sup>)–H and C(s...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
2015-2016 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe
Cross-dehydrogenative coupling (CDC) is a process in which, typically, a C–C bond is formed at the e...
In recent years, the cross-dehydrogenative coupling (CDC) has demonstrated to be a powerful syntheti...
The present review summarizes primary publications on the cross-dehydrogenative C–O coupling, with s...
This thesis describes the formation of new C-C bonds from the direct oxidative coupling ...
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 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...
Amination and amidation of aryl compounds using a transition-metal-catalyzed cross-coupling reaction...
The EPSRC and ERC are gratefully acknowledged for support. S.P.N. is a Royal Society Wolfson Researc...
An iron-catalyzed oxidative esterification reaction between unactivated C(sp<sup>3</sup>)–H bonds f...
Catalytic oxidative cross-dehydrogenative coupling between unactivated C(sp<sup>2</sup>)–H and C(s...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
2015-2016 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe
Cross-dehydrogenative coupling (CDC) is a process in which, typically, a C–C bond is formed at the e...
In recent years, the cross-dehydrogenative coupling (CDC) has demonstrated to be a powerful syntheti...
The present review summarizes primary publications on the cross-dehydrogenative C–O coupling, with s...
This thesis describes the formation of new C-C bonds from the direct oxidative coupling ...
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 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...
Amination and amidation of aryl compounds using a transition-metal-catalyzed cross-coupling reaction...
The EPSRC and ERC are gratefully acknowledged for support. S.P.N. is a Royal Society Wolfson Researc...
An iron-catalyzed oxidative esterification reaction between unactivated C(sp<sup>3</sup>)–H bonds f...
Catalytic oxidative cross-dehydrogenative coupling between unactivated C(sp<sup>2</sup>)–H and C(s...
Biaryl bonds are a common motif found in biologically active compounds and the majority of marketed ...
2015-2016 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe