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Al-Mousawi, S.M., et al. Azolylacetones as Precursors to Indoles and Naphthofurans Facilitated by Microwave Irradiation with Simultaneous Cooling. Molecules 2009, 14, 2976-2984
Molecules 2010, 15(1), 94-99; doi:10.3390/molecules15010094
Communication

Solvent Free, Microwave Assisted Conversion of Aldehydes into Nitriles and Oximes in the Presence of NH2OH·HCl and TiO2

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Received: 27 October 2009; in revised form: 22 December 2009 / Accepted: 23 December 2009 / Published: 29 December 2009
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Abstract: Aromatic aldehydes bearing electron-donating groups are easily converted into their respective nitriles using NH2OH·HCl and TiO2 under microwave irradiation, while those bearing an electron-withdrawing group give the corresponding oximes.
Keywords: titanium dioxide; aldehydes; nitriles; oximes; microwave irradiation titanium dioxide; aldehydes; nitriles; oximes; microwave irradiation
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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MDPI and ACS Style

Villas-Boas Hoelz, L.; Gonçalves, B.T.; Barros, J.C.; Mendes da Silva, J.F. Solvent Free, Microwave Assisted Conversion of Aldehydes into Nitriles and Oximes in the Presence of NH2OH·HCl and TiO2. Molecules 2010, 15, 94-99.

AMA Style

Villas-Boas Hoelz L, Gonçalves BT, Barros JC, Mendes da Silva JF. Solvent Free, Microwave Assisted Conversion of Aldehydes into Nitriles and Oximes in the Presence of NH2OH·HCl and TiO2. Molecules. 2010; 15(1):94-99.

Chicago/Turabian Style

Villas-Boas Hoelz, Lucas; Gonçalves, Biank Tomaz; Barros, José Celestino; Mendes da Silva, Joaquim Fernando. 2010. "Solvent Free, Microwave Assisted Conversion of Aldehydes into Nitriles and Oximes in the Presence of NH2OH·HCl and TiO2." Molecules 15, no. 1: 94-99.


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