Alkyne C C bond breaking, outside of alkyne metathesis, remains an underdeveloped area in reaction discovery. Recently, nitrogenation has been reported to allow nitrile formation from alkynes. A new protocol for the metal-free C C bond cleavage of terminal alkynes to produce nitriles is reported. This method provides an opportunity to synthesize a vast range of nitriles containing aryl, heteroaryl, and natural product derivatives (38 examples). In addition, the potential of tBuONO to act as a powerful nitrogenating agent for terminal aryl alkynes is demonstrated
The terminal nitride complexes NW(OC(CF3)2Me)3(DME) (1-DME), [Li(DME)2][NW(OC(CF3)2Me)4] (2), and [N...
Nitrogen-containing compounds are widely present in both natural products and synthetic compounds, f...
Recent interest in skeletal editing necessitates the continued development of reagent classes with t...
CONSPECTUS: Because of the importance of nitrogen-containing compounds in chemistry and biology, org...
Three in one blow! A novel direct transformation of alkynes into nitriles by a silver-catalyzed nitr...
A new cleavage reaction of carbon–carbon triple bonds proceeds efficiently with NIS and TMSN<sub>3</...
A metal-free PhI(OAc)<sub>2</sub> mediated nitrogenation of alkenes through CC bond cleavage using...
An NBS mediated nitriles synthesis through C=C double bond cleavage has been developed. TMSN3 was em...
A novel and efficient approach to alkenyl nitriles from readily available propargylic alcohols has b...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Nitriles are one of the most important precursors in organic synthesis. These compounds are used for...
We report the nickel-catalyzed cyanation and hydrocynation methods to prepare aryl nitriles and viny...
Nitrile is one of the ubiquitous functional groups in natural products and polymer industry. It is o...
nitrogen-containing compounds are widely present in both natural products and synthetic compounds, f...
The nitrile group is shown to direct the palladium-catalysed hydroarylation of internal alkynes bear...
The terminal nitride complexes NW(OC(CF3)2Me)3(DME) (1-DME), [Li(DME)2][NW(OC(CF3)2Me)4] (2), and [N...
Nitrogen-containing compounds are widely present in both natural products and synthetic compounds, f...
Recent interest in skeletal editing necessitates the continued development of reagent classes with t...
CONSPECTUS: Because of the importance of nitrogen-containing compounds in chemistry and biology, org...
Three in one blow! A novel direct transformation of alkynes into nitriles by a silver-catalyzed nitr...
A new cleavage reaction of carbon–carbon triple bonds proceeds efficiently with NIS and TMSN<sub>3</...
A metal-free PhI(OAc)<sub>2</sub> mediated nitrogenation of alkenes through CC bond cleavage using...
An NBS mediated nitriles synthesis through C=C double bond cleavage has been developed. TMSN3 was em...
A novel and efficient approach to alkenyl nitriles from readily available propargylic alcohols has b...
The need for precise and flexible synthetic methodology to underpin modern research in chemical biol...
Nitriles are one of the most important precursors in organic synthesis. These compounds are used for...
We report the nickel-catalyzed cyanation and hydrocynation methods to prepare aryl nitriles and viny...
Nitrile is one of the ubiquitous functional groups in natural products and polymer industry. It is o...
nitrogen-containing compounds are widely present in both natural products and synthetic compounds, f...
The nitrile group is shown to direct the palladium-catalysed hydroarylation of internal alkynes bear...
The terminal nitride complexes NW(OC(CF3)2Me)3(DME) (1-DME), [Li(DME)2][NW(OC(CF3)2Me)4] (2), and [N...
Nitrogen-containing compounds are widely present in both natural products and synthetic compounds, f...
Recent interest in skeletal editing necessitates the continued development of reagent classes with t...