Chemo- and regioselective synthesis of acyl-cyclohexenes by a tandem acceptorless dehydrogenation-[1,5]-hydride shift cascade
An atom-economical methodology to access substituted acyl-cyclohexenes from pentamethylacetophenone and 1,5-diols is described. This process is catalyzed by an iridium(I) catalyst in conjunction with a bulky electron rich phosphine ligand (CataCXium A) which favors acceptorless dehydrogenation over...
المؤلفون الرئيسيون: | Smith, L, Armstrong, R, Matheau-Raven, D, Donohoe, T |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
American Chemical Society
2020
|
مواد مشابهة
-
Acceptorless and base-free dehydrogenation of alcohols and amines using ruthenium-hydride complexes
حسب: Muthaiah, Senthilkumar, وآخرون
منشور في: (2013) -
Catalytic acceptorless complete dehydrogenation of cycloalkanes
حسب: Rahul A. Jagtap, وآخرون
منشور في: (2025-01-01) -
Iron-based nanocatalyst for the acceptorless dehydrogenation reactions
حسب: Garima Jaiswal, وآخرون
منشور في: (2017-12-01) -
Redox reorganization: aluminium promoted 1,5-hydride shifts allow the controlled synthesis of multisubstituted cyclohexenes
حسب: Smith, LB, وآخرون
منشور في: (2023) -
Identification of active catalysts for the acceptorless dehydrogenation of alcohols to carbonyls
حسب: Tao Wang, وآخرون
منشور في: (2021-08-01)