An operationally simple and high-yielding procedure was developed for the conversion of aryl aldehydes into the corresponding nitriles using p-toluenesulfonic acid as a mild catalyst under microwave irradn. The products were characterized by IR spectral anal. and by comparison of the melting and b.ps. with the reported values
A mixture of bismuth nitrate pentahydrate and potassium aryltrifluoroborate in toluene under microwa...
Nitriles are of importance as very useful starting materials for the synthesis of a variety of biolo...
The Schmidt reaction of aromatic aldehydes using a substoichiometric amount (40 mol %) of triflic ac...
Zinc chloride has been found to be an excellent catalyst for a one-pot synthesis of nitriles from ar...
A rapid and facile method for the conversion of primary amides to nitriles using inexpensive and rea...
A rapid and eco-friendly one-pot protocol for the synthesis of nitriles has been developed by treati...
Nitriles are versatile organic precursors in organic synthesis and have numerous applications. An ef...
A simple and convenient one - pot protocol for preparing nitriles by treating different aromatic ald...
Aldehydes are converted into corresponding nitriles in high yields by a one-pot solvent-free reactio...
This work is licensed under a Creative Commons Attribution 4.0 International License.The Schmidt rea...
14 Azalactones were synthesized in excellent yields under solvent-free conditions by heating an ald...
1025-1029The method of microwave-assisted synthesis of benzylidenemalononitrile and its derivatives ...
This work is licensed under a Creative Commons Attribution 4.0 International License.The Schmidt rea...
The method of microwave-assisted synthesis of benzylidenemalononitrile and its derivatives by using ...
The Schmidt reaction of aromatic aldehydes using a substoichiometric amount (40 mol %) of triflic ac...
A mixture of bismuth nitrate pentahydrate and potassium aryltrifluoroborate in toluene under microwa...
Nitriles are of importance as very useful starting materials for the synthesis of a variety of biolo...
The Schmidt reaction of aromatic aldehydes using a substoichiometric amount (40 mol %) of triflic ac...
Zinc chloride has been found to be an excellent catalyst for a one-pot synthesis of nitriles from ar...
A rapid and facile method for the conversion of primary amides to nitriles using inexpensive and rea...
A rapid and eco-friendly one-pot protocol for the synthesis of nitriles has been developed by treati...
Nitriles are versatile organic precursors in organic synthesis and have numerous applications. An ef...
A simple and convenient one - pot protocol for preparing nitriles by treating different aromatic ald...
Aldehydes are converted into corresponding nitriles in high yields by a one-pot solvent-free reactio...
This work is licensed under a Creative Commons Attribution 4.0 International License.The Schmidt rea...
14 Azalactones were synthesized in excellent yields under solvent-free conditions by heating an ald...
1025-1029The method of microwave-assisted synthesis of benzylidenemalononitrile and its derivatives ...
This work is licensed under a Creative Commons Attribution 4.0 International License.The Schmidt rea...
The method of microwave-assisted synthesis of benzylidenemalononitrile and its derivatives by using ...
The Schmidt reaction of aromatic aldehydes using a substoichiometric amount (40 mol %) of triflic ac...
A mixture of bismuth nitrate pentahydrate and potassium aryltrifluoroborate in toluene under microwa...
Nitriles are of importance as very useful starting materials for the synthesis of a variety of biolo...
The Schmidt reaction of aromatic aldehydes using a substoichiometric amount (40 mol %) of triflic ac...