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Au/Ag-Cocatalyzed aldoximes to amides rearrangement under solvent- and acid-free conditions

Ruben S Ramon, Johann Bosson, Silvia Diez-Gonzalez, Nicolas Marion and Steven Nolan (UGent)
(2010) JOURNAL OF ORGANIC CHEMISTRY. 75(4). p.1197-1202
Author
Organization
Abstract
The gold/silver-cocatalyzed conversion of aldoximes into primary amides is reported. The reaction, which proceeds under neat and acid-free conditions, allows for the conversion of a range of aldoximes, and is a rare example of cooperative catalysis involving well-defined gold species.
Keywords
N-HETEROCYCLIC CARBENES, ONE-POT, BECKMANN REARRANGEMENT, ORGANIC TRANSFORMATIONS, CATALYZED CONVERSION, HYDROXIDE CATALYST, HIGHLY EFFICIENT, GOLD CATALYSIS, NITRILES, DEHYDRATION

Citation

Please use this url to cite or link to this publication:

MLA
Ramon, Ruben S., et al. “Au/Ag-Cocatalyzed Aldoximes to Amides Rearrangement under Solvent- and Acid-Free Conditions.” JOURNAL OF ORGANIC CHEMISTRY, vol. 75, no. 4, 2010, pp. 1197–202.
APA
Ramon, R. S., Bosson, J., Diez-Gonzalez, S., Marion, N., & Nolan, S. (2010). Au/Ag-Cocatalyzed aldoximes to amides rearrangement under solvent- and acid-free conditions. JOURNAL OF ORGANIC CHEMISTRY, 75(4), 1197–1202.
Chicago author-date
Ramon, Ruben S, Johann Bosson, Silvia Diez-Gonzalez, Nicolas Marion, and Steven Nolan. 2010. “Au/Ag-Cocatalyzed Aldoximes to Amides Rearrangement under Solvent- and Acid-Free Conditions.” JOURNAL OF ORGANIC CHEMISTRY 75 (4): 1197–1202.
Chicago author-date (all authors)
Ramon, Ruben S, Johann Bosson, Silvia Diez-Gonzalez, Nicolas Marion, and Steven Nolan. 2010. “Au/Ag-Cocatalyzed Aldoximes to Amides Rearrangement under Solvent- and Acid-Free Conditions.” JOURNAL OF ORGANIC CHEMISTRY 75 (4): 1197–1202.
Vancouver
1.
Ramon RS, Bosson J, Diez-Gonzalez S, Marion N, Nolan S. Au/Ag-Cocatalyzed aldoximes to amides rearrangement under solvent- and acid-free conditions. JOURNAL OF ORGANIC CHEMISTRY. 2010;75(4):1197–202.
IEEE
[1]
R. S. Ramon, J. Bosson, S. Diez-Gonzalez, N. Marion, and S. Nolan, “Au/Ag-Cocatalyzed aldoximes to amides rearrangement under solvent- and acid-free conditions,” JOURNAL OF ORGANIC CHEMISTRY, vol. 75, no. 4, pp. 1197–1202, 2010.
@article{8169301,
  abstract     = {The gold/silver-cocatalyzed conversion of aldoximes into primary amides is reported. The reaction, which proceeds under neat and acid-free conditions, allows for the conversion of a range of aldoximes, and is a rare example of cooperative catalysis involving well-defined gold species.},
  author       = {Ramon, Ruben S and Bosson, Johann and Diez-Gonzalez, Silvia and Marion, Nicolas and Nolan, Steven},
  issn         = {0022-3263},
  journal      = {JOURNAL OF ORGANIC CHEMISTRY},
  keywords     = {N-HETEROCYCLIC CARBENES,ONE-POT,BECKMANN REARRANGEMENT,ORGANIC TRANSFORMATIONS,CATALYZED CONVERSION,HYDROXIDE CATALYST,HIGHLY EFFICIENT,GOLD CATALYSIS,NITRILES,DEHYDRATION},
  language     = {eng},
  number       = {4},
  pages        = {1197--1202},
  title        = {Au/Ag-Cocatalyzed aldoximes to amides rearrangement under solvent- and acid-free conditions},
  url          = {http://dx.doi.org/10.1021/jo902461a},
  volume       = {75},
  year         = {2010},
}
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