Literature DB >> 17889529

Highly efficient selective oxidation of alcohols to carbonyl compounds catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen.

Hong-Bing Ji1, Qiu-Lan Yuan, Xian-Tai Zhou, Li-Xia Pei, Le-Fu Wang.   

Abstract

Efficient selective oxidation of alcohols to carbonyl compounds by molecular oxygen with isobutyraldehyde as oxygen acceptor in the presence of metalloporphyrins has been reported. Ruthenium (III) meso-tetraphenylporphyrin chloride (Ru(TPP)Cl) showed excellent activity and selectivity for oxidation of various alcohols under mild conditions. Moreover, different factors influencing alcohols oxidation, for example, catalyst, solvent, temperature, and oxidant, have been investigated. In large-scale oxidation of benzyl alcohol, the isolated yield of benzaldehyde of 89% was observed.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17889529     DOI: 10.1016/j.bmcl.2007.08.063

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Metal-free activation of H₂O₂ by synergic effect of ionic liquid and microwave: chemoselective oxidation of benzylic alcohols to carbonyls and unexpected formation of anthraquinone in aqueous condition.

Authors:  Rakesh Kumar; Nandini Sharma; Naina Sharma; Abhishek Sharma; Arun K Sinha
Journal:  Mol Divers       Date:  2010-11-28       Impact factor: 2.943

2.  Selective oxidation of alcohols and sulfides via O2 using a Co(ii) salen complex catalyst immobilized on KCC-1: synthesis and kinetic study.

Authors:  Ali Allahresani; Elaheh Naghdi; Mohammad Ali Nasseri; Kaveh Hemmat
Journal:  RSC Adv       Date:  2020-10-14       Impact factor: 4.036

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.