A facile protocol for the synthesis of quinoline formaldehydes via direct oxidative C–H bonds functionalization of methyl-azaheteroarenes in the presence of I2–DMSO has been described. This method is metal-free and easy to operate. This reaction provided a convenient route for the preparation of a range of important quinoline formaldehydes.The accepted manuscript in pdf format is listed with the files at the bottom of this page. The presentation of the authors' names and (or) special characters in the title of the manuscript may differ slightly between what is listed on this page and what is listed in the pdf file of the accepted manuscript; that in the pdf file of the accepted manuscript is what was submitted by the author
Functionalization of C(sp3)−H bonds under metal-free reaction conditions is a great challenge due to...
M. Sc. University of KwaZulu-Natal, Pietermaritzburg 2016.Quinolines play an important role in organ...
Stille coupling on N-(2-iodo-phenyl)-acetamide followed by reduction-deprotection sequence has been ...
A facile protocol for the synthesis of quinoline formaldehydes via direct oxidative C–H bonds functi...
A transition-metal-free method for the construction of 3-substituted or 3,4-disubstituted quinolines...
The development of novel and efficient methods for the transition metal-free functionalization of in...
An expedient and metal-free synthetic protocol for construction of substituted quinolines has been d...
An efficient and practical iodine-catalyzed oxidative functionalization of azaarenes with benzylic C...
An efficient method for the direct synthesis of substituted quinolines from anilines and aldehydes t...
Dehalogenation of а series substituted 2-chloroquinoline-3-carbaldehydes was investigated. It was fo...
A novel, metal-free oxidative intramolecular Mannich reaction was developed between secondary amines...
A highly efficient metal and protection-free approach for the regioselective synthesis of C-3-functi...
A novel and convenient method has been developed for the regioselective iodination of quinolines at ...
Metal free dehydrogenation of various substituted tetrahydroisoquinolines via a simple and convenien...
Dess–Martin periodinane (DMP) is a broadly applicable oxidant in chemical synthesis. In this work, a...
Functionalization of C(sp3)−H bonds under metal-free reaction conditions is a great challenge due to...
M. Sc. University of KwaZulu-Natal, Pietermaritzburg 2016.Quinolines play an important role in organ...
Stille coupling on N-(2-iodo-phenyl)-acetamide followed by reduction-deprotection sequence has been ...
A facile protocol for the synthesis of quinoline formaldehydes via direct oxidative C–H bonds functi...
A transition-metal-free method for the construction of 3-substituted or 3,4-disubstituted quinolines...
The development of novel and efficient methods for the transition metal-free functionalization of in...
An expedient and metal-free synthetic protocol for construction of substituted quinolines has been d...
An efficient and practical iodine-catalyzed oxidative functionalization of azaarenes with benzylic C...
An efficient method for the direct synthesis of substituted quinolines from anilines and aldehydes t...
Dehalogenation of а series substituted 2-chloroquinoline-3-carbaldehydes was investigated. It was fo...
A novel, metal-free oxidative intramolecular Mannich reaction was developed between secondary amines...
A highly efficient metal and protection-free approach for the regioselective synthesis of C-3-functi...
A novel and convenient method has been developed for the regioselective iodination of quinolines at ...
Metal free dehydrogenation of various substituted tetrahydroisoquinolines via a simple and convenien...
Dess–Martin periodinane (DMP) is a broadly applicable oxidant in chemical synthesis. In this work, a...
Functionalization of C(sp3)−H bonds under metal-free reaction conditions is a great challenge due to...
M. Sc. University of KwaZulu-Natal, Pietermaritzburg 2016.Quinolines play an important role in organ...
Stille coupling on N-(2-iodo-phenyl)-acetamide followed by reduction-deprotection sequence has been ...