A convenient strategy for the synthesis of sulfur ylides via rhodium-catalyzed coupling of in situ generated iodonium ylides with sulfides or sulfoxides has been developed. A wide range of sulfur ylides were obtained in moderate to good yields from inexpensive sulfur compounds and active methylene compounds with a short reaction time (MW, 5–10 min) or 12–16 h at rt. Furthermore, these sulfoxonium ylides were used as novel acceptor/acceptor carbenes for N–H insertion reactions
A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation o...
This thesis documents the development of synthetic methodologies utilising rhodium catalysis for the...
Sulfur-containing molecules are commonly found in chemical biology, organic synthesis, and materials...
Iodonium ylides are attractive and important reagents in organic synthesis.1 Iodonium ylides are als...
The functionalization of carbon-hydrogen bonds in non-nucleophilic substrates using α-carbonyl sulfo...
Sulfoxonium ylides have recently gained prominence as safe carbenoid precursors in metal-catalyzed r...
Chemodivergent and redox-neutral annulations between N-methoxybenzamides and sulfoxonium ylides have...
Sulfoxonium ylides act as an efficient carbene precursor in rhodium(III)-catalyzed C–H acylmethlyat...
Vinylsulfonates have proved to be excellent dipolarophiles for carbonyl ylides derived from diazoket...
Sulfur ylides first disclosed in 1930 started to gain more attention in the 1960s, thanks mainly to ...
Sulfur ylides first disclosed in 1930 started to gain more attention in the 1960s, thanks mainly to ...
Sulfur ylides first disclosed in 1930 started to gain more attention in the 1960s, thanks mainly to ...
A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation o...
Direct and efficient synthesis of 1-naphthols has been realized via Rh(III)-catalyzed C-H activation...
Direct and efficient synthesis of 1-naphthols has been realized via Rh(III)-catalyzed C-H activation...
A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation o...
This thesis documents the development of synthetic methodologies utilising rhodium catalysis for the...
Sulfur-containing molecules are commonly found in chemical biology, organic synthesis, and materials...
Iodonium ylides are attractive and important reagents in organic synthesis.1 Iodonium ylides are als...
The functionalization of carbon-hydrogen bonds in non-nucleophilic substrates using α-carbonyl sulfo...
Sulfoxonium ylides have recently gained prominence as safe carbenoid precursors in metal-catalyzed r...
Chemodivergent and redox-neutral annulations between N-methoxybenzamides and sulfoxonium ylides have...
Sulfoxonium ylides act as an efficient carbene precursor in rhodium(III)-catalyzed C–H acylmethlyat...
Vinylsulfonates have proved to be excellent dipolarophiles for carbonyl ylides derived from diazoket...
Sulfur ylides first disclosed in 1930 started to gain more attention in the 1960s, thanks mainly to ...
Sulfur ylides first disclosed in 1930 started to gain more attention in the 1960s, thanks mainly to ...
Sulfur ylides first disclosed in 1930 started to gain more attention in the 1960s, thanks mainly to ...
A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation o...
Direct and efficient synthesis of 1-naphthols has been realized via Rh(III)-catalyzed C-H activation...
Direct and efficient synthesis of 1-naphthols has been realized via Rh(III)-catalyzed C-H activation...
A highly efficient Rh-catalyzed carbenoid addition to trifluoromethylthioether for the formation o...
This thesis documents the development of synthetic methodologies utilising rhodium catalysis for the...
Sulfur-containing molecules are commonly found in chemical biology, organic synthesis, and materials...