An efficient, catalyst-free, and metal-free bromoamidation of unactivated olefins has been developed. 4-(Trifluoromethyl)benzenesulfonamide and <i>N</i>-bromosuccinimide were used as the nitrogen and halogen sources, respectively. The methodology is applicable to both cyclic and aliphatic olefins
Functional group tolerance is one of the important requirements for chemical reactions, especially f...
An asymmetric intermolecular bromoesterification of unfunctionalized olefins catalyzed by (DHQD)<sub...
A new method of brominating aromatic and heteroaromatic ring systems is investigated. The combinati...
An efficient, catalyst-free, and metal-free bromoamidation of unactivated olefins has been developed...
Herein, we report the first metal-free and molecular halogen reagent-free dihomohalogenation methodo...
Highly deactivated aromatic compounds were smoothly monobrominated by treatment with N-bromosuccinim...
A metal-free method for intramolecular halocyclization of unfunctionalized olefins was detailed. (Di...
The bromonium-promoted cyclization of conjugated aminodienes is described. The reaction proceeds smo...
Anilines are key constituents in biologically active compounds and often obtained from transition me...
A highly practical copper-catalyzed intermolecular halotrifluoromethylation of alkenes has been de...
AbstractA highly efficient method for the synthesis of α-halocarbonyl compounds has been achieved vi...
Microwave-induced solvent-free brominations of organic substrates have been carried out with tetrabu...
<i>N</i>,<i>N</i>-Dibromo-<i>p</i>-toluene sulfonamide (TsNBr<sub>2</sub>) has been found to be an e...
A palladium catalyzed Negishi-type α-arylation of sulfones and sulfonamides with a broad range of ar...
Bromination of 2,7-dinitro-9,10-phenanthrenequinone, 2,5-dinitro-9,10- phenanthrenequinone, and 2,4,...
Functional group tolerance is one of the important requirements for chemical reactions, especially f...
An asymmetric intermolecular bromoesterification of unfunctionalized olefins catalyzed by (DHQD)<sub...
A new method of brominating aromatic and heteroaromatic ring systems is investigated. The combinati...
An efficient, catalyst-free, and metal-free bromoamidation of unactivated olefins has been developed...
Herein, we report the first metal-free and molecular halogen reagent-free dihomohalogenation methodo...
Highly deactivated aromatic compounds were smoothly monobrominated by treatment with N-bromosuccinim...
A metal-free method for intramolecular halocyclization of unfunctionalized olefins was detailed. (Di...
The bromonium-promoted cyclization of conjugated aminodienes is described. The reaction proceeds smo...
Anilines are key constituents in biologically active compounds and often obtained from transition me...
A highly practical copper-catalyzed intermolecular halotrifluoromethylation of alkenes has been de...
AbstractA highly efficient method for the synthesis of α-halocarbonyl compounds has been achieved vi...
Microwave-induced solvent-free brominations of organic substrates have been carried out with tetrabu...
<i>N</i>,<i>N</i>-Dibromo-<i>p</i>-toluene sulfonamide (TsNBr<sub>2</sub>) has been found to be an e...
A palladium catalyzed Negishi-type α-arylation of sulfones and sulfonamides with a broad range of ar...
Bromination of 2,7-dinitro-9,10-phenanthrenequinone, 2,5-dinitro-9,10- phenanthrenequinone, and 2,4,...
Functional group tolerance is one of the important requirements for chemical reactions, especially f...
An asymmetric intermolecular bromoesterification of unfunctionalized olefins catalyzed by (DHQD)<sub...
A new method of brominating aromatic and heteroaromatic ring systems is investigated. The combinati...