The site-selective C8-alkylation of quinolines has been accomplished using cyclopropyl alcohols as the alkylating agents and N-oxide as a weak chelating group in the presence of Co(III) catalysis via merging C–H/C–C bond activation. The use of cyclopropanol as the alkyl source, Co catalysis, substrate scope, HRMS analysis of the reaction intermediate, and late-stage mutation of drug molecules/natural products are the important practical features
Organomercurial esters 2a-c obtained from cyclopropyl alcohols la-c in three or five (depending on w...
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline N-oxides has bee...
Carbon-carbon sigma bonds are known to be very stable under most reaction conditions; however, throu...
The activation of C-C bonds in organic molecules is one of current interests in organometallic chemi...
The synthesis of isoquinolines by site-selective CH activation of O-acyl oximes with a Cp*Co-III cat...
This thesis describes new methods for C–O and C–C functionalization in the contexts of cyclopropanol...
A bidentate chelation-assisted cobalt-catalyzed C(sp2)–H activation and annulation of benzamides an...
Cobalt–diphosphine catalysts promote ring-opening coupling reactions between cyclopropanols and unac...
An efficient synthesis of 2-substituted quinolines from readily available cyclopropanols and imidami...
Quinoline is a versatile heterocycle that is part of numerous natural products and countless drugs. ...
C2- and C5-alkynylated quinolone scaffolds are core structures of numerous biologically active molec...
A weakly coordinating biorelevant intrinsic directing group (DG) assisted site-selective C–H alkenyl...
A facile and efficient protocol for palladium-catalyzed C8-selective acylation of quinoline <i>N</i>...
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline <i>N</i>-oxides...
Under Rh-catalyzed conditions, secondary amines and anilines function as directing groups to facilit...
Organomercurial esters 2a-c obtained from cyclopropyl alcohols la-c in three or five (depending on w...
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline N-oxides has bee...
Carbon-carbon sigma bonds are known to be very stable under most reaction conditions; however, throu...
The activation of C-C bonds in organic molecules is one of current interests in organometallic chemi...
The synthesis of isoquinolines by site-selective CH activation of O-acyl oximes with a Cp*Co-III cat...
This thesis describes new methods for C–O and C–C functionalization in the contexts of cyclopropanol...
A bidentate chelation-assisted cobalt-catalyzed C(sp2)–H activation and annulation of benzamides an...
Cobalt–diphosphine catalysts promote ring-opening coupling reactions between cyclopropanols and unac...
An efficient synthesis of 2-substituted quinolines from readily available cyclopropanols and imidami...
Quinoline is a versatile heterocycle that is part of numerous natural products and countless drugs. ...
C2- and C5-alkynylated quinolone scaffolds are core structures of numerous biologically active molec...
A weakly coordinating biorelevant intrinsic directing group (DG) assisted site-selective C–H alkenyl...
A facile and efficient protocol for palladium-catalyzed C8-selective acylation of quinoline <i>N</i>...
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline <i>N</i>-oxides...
Under Rh-catalyzed conditions, secondary amines and anilines function as directing groups to facilit...
Organomercurial esters 2a-c obtained from cyclopropyl alcohols la-c in three or five (depending on w...
The Rh(III)-catalyzed C-8 selective direct alkylation and alkynylation of quinoline N-oxides has bee...
Carbon-carbon sigma bonds are known to be very stable under most reaction conditions; however, throu...