A new protocol for the synthesis of nitriles from carbonyl compounds with elongation of the molecule with two carbon atoms was developed. It involves a reaction of ethyl cyanoacetate with different aldehydes in the presence of iron pentacarbonyl as a reducing agent. This protocol is very simple and requires only commonly available reagents, with no catalyst or complicated ligands being employed. © 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinhei
The nitrile is an extremely useful functional group in organic synthesis: it can be transformed into...
Transition-metal-free synthesis of alpha-aryl esters and nitriles using arylboronic acids with alpha...
Carbon-Carbon cross-coupling is a useful method that is used to connect carbons of different molecul...
CONSPECTUS: Because of the importance of nitrogen-containing compounds in chemistry and biology, org...
Nitrile is one of the ubiquitous functional groups in natural products and polymer industry. It is o...
Nitriles are one of the most important precursors in organic synthesis. These compounds are used for...
1000-1006Aldehydes are converted into nitriles in a one-pot reaction by treatment with H2NOH.HCl i...
The preparation of a number of 2-cyanostyrene derivatives by the condensation of methyleneaminoaceto...
Aldehydes are converted into nitriles in a one-pot reaction by treatment with H2NOH.HCl in dipolar a...
A rapid and eco-friendly one-pot protocol for the synthesis of nitriles has been developed by treati...
Cyanide addition to cyclopentadienyliron complexes of substituted nitroarenes produced nitrile adduc...
Through a nickel-catalysed Heck-type reaction, a direct coupling of alkenes with alpha-cyano alkyl b...
The three title reductant systems have significant advantages in generating aldehydes fromnitriles. ...
A current challenge in catalysis is the development of methodologies for the production of bulk chem...
Michael addition of malononitrile as nucleophiles to nitroalkenes as electrophiles has been scarcely...
The nitrile is an extremely useful functional group in organic synthesis: it can be transformed into...
Transition-metal-free synthesis of alpha-aryl esters and nitriles using arylboronic acids with alpha...
Carbon-Carbon cross-coupling is a useful method that is used to connect carbons of different molecul...
CONSPECTUS: Because of the importance of nitrogen-containing compounds in chemistry and biology, org...
Nitrile is one of the ubiquitous functional groups in natural products and polymer industry. It is o...
Nitriles are one of the most important precursors in organic synthesis. These compounds are used for...
1000-1006Aldehydes are converted into nitriles in a one-pot reaction by treatment with H2NOH.HCl i...
The preparation of a number of 2-cyanostyrene derivatives by the condensation of methyleneaminoaceto...
Aldehydes are converted into nitriles in a one-pot reaction by treatment with H2NOH.HCl in dipolar a...
A rapid and eco-friendly one-pot protocol for the synthesis of nitriles has been developed by treati...
Cyanide addition to cyclopentadienyliron complexes of substituted nitroarenes produced nitrile adduc...
Through a nickel-catalysed Heck-type reaction, a direct coupling of alkenes with alpha-cyano alkyl b...
The three title reductant systems have significant advantages in generating aldehydes fromnitriles. ...
A current challenge in catalysis is the development of methodologies for the production of bulk chem...
Michael addition of malononitrile as nucleophiles to nitroalkenes as electrophiles has been scarcely...
The nitrile is an extremely useful functional group in organic synthesis: it can be transformed into...
Transition-metal-free synthesis of alpha-aryl esters and nitriles using arylboronic acids with alpha...
Carbon-Carbon cross-coupling is a useful method that is used to connect carbons of different molecul...