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Iridium(I) hydroxides in catalysis : rearrangement of allylic alcohols to ketones

(2014) ORGANIC & BIOMOLECULAR CHEMISTRY. 12(34). p.6672-6676
Author
Organization
Abstract
The iridium(I) hydroxide complex [Ir(OH)(COD)((IPr)-Pr-i)] has been shown to be a competent catalyst for the rearrangement of allylic alcohols to ketones. Reactions proceed in short reaction times (1-1.5 h) with microwave heating, in the absence of additives.
Keywords
TRANSITION-METAL-COMPLEXES, CARBONYL-COMPOUNDS, ISOMERIZATION, PARAMETERS

Citation

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

MLA
Nelson, David J., et al. “Iridium(I) Hydroxides in Catalysis : Rearrangement of Allylic Alcohols to Ketones.” ORGANIC & BIOMOLECULAR CHEMISTRY, vol. 12, no. 34, 2014, pp. 6672–76.
APA
Nelson, D. J., Fernandez-Salas, J. A., Truscott, B. J., & Nolan, S. (2014). Iridium(I) hydroxides in catalysis : rearrangement of allylic alcohols to ketones. ORGANIC & BIOMOLECULAR CHEMISTRY, 12(34), 6672–6676.
Chicago author-date
Nelson, David J, Jose A Fernandez-Salas, Byron J Truscott, and Steven Nolan. 2014. “Iridium(I) Hydroxides in Catalysis : Rearrangement of Allylic Alcohols to Ketones.” ORGANIC & BIOMOLECULAR CHEMISTRY 12 (34): 6672–76.
Chicago author-date (all authors)
Nelson, David J, Jose A Fernandez-Salas, Byron J Truscott, and Steven Nolan. 2014. “Iridium(I) Hydroxides in Catalysis : Rearrangement of Allylic Alcohols to Ketones.” ORGANIC & BIOMOLECULAR CHEMISTRY 12 (34): 6672–6676.
Vancouver
1.
Nelson DJ, Fernandez-Salas JA, Truscott BJ, Nolan S. Iridium(I) hydroxides in catalysis : rearrangement of allylic alcohols to ketones. ORGANIC & BIOMOLECULAR CHEMISTRY. 2014;12(34):6672–6.
IEEE
[1]
D. J. Nelson, J. A. Fernandez-Salas, B. J. Truscott, and S. Nolan, “Iridium(I) hydroxides in catalysis : rearrangement of allylic alcohols to ketones,” ORGANIC & BIOMOLECULAR CHEMISTRY, vol. 12, no. 34, pp. 6672–6676, 2014.
@article{8168560,
  abstract     = {The iridium(I) hydroxide complex [Ir(OH)(COD)((IPr)-Pr-i)] has been shown to be a competent catalyst for the rearrangement of allylic alcohols to ketones. Reactions proceed in short reaction times (1-1.5 h) with microwave heating, in the absence of additives.},
  author       = {Nelson, David J and Fernandez-Salas, Jose A and Truscott, Byron J and Nolan, Steven},
  issn         = {1477-0520},
  journal      = {ORGANIC & BIOMOLECULAR CHEMISTRY},
  keywords     = {TRANSITION-METAL-COMPLEXES,CARBONYL-COMPOUNDS,ISOMERIZATION,PARAMETERS},
  language     = {eng},
  number       = {34},
  pages        = {6672--6676},
  title        = {Iridium(I) hydroxides in catalysis : rearrangement of allylic alcohols to ketones},
  url          = {http://dx.doi.org/10.1039/c4ob01428f},
  volume       = {12},
  year         = {2014},
}

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