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Switchable Chemoselective Transfer Hydrogenations of Unsaturated Carbonyls Using Copper(I) N-Donor Thiolate Clusters.
Zhang, Meng-Juan; Tan, Da-Wei; Li, Hong-Xi; Young, David James; Wang, Hui-Fang; Li, Hai-Yan; Lang, Jian-Ping.
Afiliación
  • Zhang MJ; College of Chemistry, Chemical Engineering and Materials Science, Soochow University , Suzhou 215123 Jiangsu, People's Republic of China.
  • Tan DW; College of Chemistry, Chemical Engineering and Materials Science, Soochow University , Suzhou 215123 Jiangsu, People's Republic of China.
  • Li HX; College of Chemistry, Chemical Engineering and Materials Science, Soochow University , Suzhou 215123 Jiangsu, People's Republic of China.
  • Young DJ; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , Shanghai 200032, People's Republic of China.
  • Wang HF; Faculty of Science and Engineering, University of the Sunshine Coast , Maroochydore DC, Queensland 4558, Australia.
  • Li HY; College of Chemistry, Chemical Engineering and Materials Science, Soochow University , Suzhou 215123 Jiangsu, People's Republic of China.
  • Lang JP; College of Chemistry, Chemical Engineering and Materials Science, Soochow University , Suzhou 215123 Jiangsu, People's Republic of China.
J Org Chem ; 83(3): 1204-1215, 2018 02 02.
Article en En | MEDLINE | ID: mdl-29313338
Unsaturated alcohols and saturated carbonyls are important chemical, pharmaceutical, and biochemical intermediates. We herein report an efficient transfer hydrogenation protocol in which conversion of unsaturated carbonyl compounds to either unsaturated alcohols or saturated carbonyls was catalyzed by Cu(I) N-donor thiolate clusters along with changing hydrogen source (isopropanol or butanol) and base (NaOH or K2CO3). Mechanistic studies supported by DFT transition state modeling indicate that such a chemoselectivity can be explained by the relative concentrations of Cu(I) monohydride and protonated Cu(I) hydride complexes in each catalytic system.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2018 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2018 Tipo del documento: Article