The first example of a practical and selective azidation of unactivated aliphatic C–H bonds with easily handled sulfonyl azides as azide source without the use of transition metals has been explored. This method is operationally simple, scalable, and applicable to late-stage azidation of natural products and derivatives, which make it a valuable method for the synthesis of organic azides
We report a manganese-catalyzed aliphatic C–H azidation reaction that can efficiently convert second...
Many enzymes oxidize unactivated aliphatic C-H bonds selectively to form alcohols; however, biologic...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...
A persulfate induced radical process to transform aliphatic tertiary C-H bonds into organic azides u...
The development of novel and efficient methods for the transition metal-free functionalization of in...
A novel and facile oxyazidation of alkenes under metal-free and mild conditions has been reported. A...
The azide moiety is a desirable functionality in organic molecules, useful in a variety of transform...
A wide range of methodologies for the preparation of organic azides has been reported in the literat...
A novel and environmentally attractive C(sp3)–H azidation of 2-oxindoles involving the formation of...
A simple, efficient, stereoselective, and in some cases usefully nonregioselective method for the sy...
A metal-free PhI(OAc)2-mediated method for the synthesis of acyl azides through oxidative cleavage ...
A versatile metal-free synthesis of allylic <i>N</i>-heterocycles has been developed using a TBAI/TB...
An efficient rhodium-catalyzed regioselective C–N bond formation of azo compounds in good to excelle...
Selective functionalization of complex scaffolds is a promising approach to alter the pharmacologica...
By employing a simple, inexpensive, and transition-metal-free oxidation system, secondary C–H bonds ...
We report a manganese-catalyzed aliphatic C–H azidation reaction that can efficiently convert second...
Many enzymes oxidize unactivated aliphatic C-H bonds selectively to form alcohols; however, biologic...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...
A persulfate induced radical process to transform aliphatic tertiary C-H bonds into organic azides u...
The development of novel and efficient methods for the transition metal-free functionalization of in...
A novel and facile oxyazidation of alkenes under metal-free and mild conditions has been reported. A...
The azide moiety is a desirable functionality in organic molecules, useful in a variety of transform...
A wide range of methodologies for the preparation of organic azides has been reported in the literat...
A novel and environmentally attractive C(sp3)–H azidation of 2-oxindoles involving the formation of...
A simple, efficient, stereoselective, and in some cases usefully nonregioselective method for the sy...
A metal-free PhI(OAc)2-mediated method for the synthesis of acyl azides through oxidative cleavage ...
A versatile metal-free synthesis of allylic <i>N</i>-heterocycles has been developed using a TBAI/TB...
An efficient rhodium-catalyzed regioselective C–N bond formation of azo compounds in good to excelle...
Selective functionalization of complex scaffolds is a promising approach to alter the pharmacologica...
By employing a simple, inexpensive, and transition-metal-free oxidation system, secondary C–H bonds ...
We report a manganese-catalyzed aliphatic C–H azidation reaction that can efficiently convert second...
Many enzymes oxidize unactivated aliphatic C-H bonds selectively to form alcohols; however, biologic...
We report the direct amidation of arene C–H bonds using sulfonyl azides as the amino source to relea...