Synlett

An efficient new procedure for the one-pot conversion of aldehydes into the corresponding nitriles

JL Zhu, FY Lee, JD Wu, CW Kuo, KS Shia

Index: Zhu, Jia-Liang; Lee, Fa-Yen; Wu, Jen-Dar; Kuo, Chun-Wei; Shia, Kak-Shan Synlett, 2007 , # 8 p. 1317 - 1319

Full Text: HTML

Citation Number: 20

Abstract

Abstract A new and efficient procedure for the one-pot conversion of various aldehydes into the corresponding nitriles under mild reaction conditions has been developed. The ethyl dichlorophosphate/DBU-mediated dehydration of aldoxime intermediates was utilized as a key operation to effect the transformation.

Related Articles:

A Simple Synthesis of Nitriles from Aldoximes (1)

[Coskun, Necdet Synthetic Communications, 2004 , vol. 34, # 9 p. 1625 - 1630]

One-pot conversion of aromatic bromides and aromatics into aromatic nitriles via aryllithiums and their DMF adduct

[Ushijima, Sousuke; Moriyama, Katsuhiko; Togo, Hideo Tetrahedron, 2011 , vol. 67, # 5 p. 958 - 964]

Mild and Efficient Copper??Catalyzed Cyanation of Aryl Iodides and Bromides

[Cristau, Henri-Jean; Ouali, Armelle; Spindler, Jean-Francis; Taillefer, Marc Chemistry - A European Journal, 2005 , vol. 11, # 8 p. 2483 - 2492]

A non-metal catalysed oxidation of primary azides to nitriles at ambient temperature

[Lamani, Manjunath; Devadig, Pradeep; Prabhu, Kandikere Ramaiah Organic and Biomolecular Chemistry, 2012 , vol. 10, # 14 p. 2753 - 2759]

Efficient Transformation of Aldoximes to Nitriles Using 2??Chloro??1??methylpyridinium Iodide Under Mild Conditions

[Lee, Kieseung; Han, Sang-Bae; Yoo, Eun-Mi; Chung, Soon-Ryang; Oh, Haibum; Hong, Sungwan Synthetic Communications, 2004 , vol. 34, # 10 p. 1775 - 1782]

More Articles...