20657-32-3Relevant articles and documents
Photocatalyst-free visible light promoted: E → Z isomerization of alkenes
Xu, Jianbin,Liu, Na,Lv, Haiping,He, Chixian,Liu, Zining,Shen, Xianfu,Cheng, Feixiang,Fan, Baomin
supporting information, p. 2739 - 2743 (2020/06/17)
A simple and green method of visible light driven photocatalytic E to Z isomerization of alkenes has been developed. A variety of (Z)-alkenes can be prepared in the presence of visible light, without any additional photocatalyst. This protocol features photocatalyst-free conditions, which are mild, tolerant, and operationally simple, and is easy to implement.
Immobilization and continuous recycling of photoredox catalysts in ionic liquids for applications in batch reactions and flow systems: Catalytic alkene isomerization by using visible light
Fabry, David C.,Ronge, Meria A.,Rueping, Magnus
supporting information, p. 5350 - 5354 (2015/03/30)
A catalytic (E)- to (Z)-isomerization of olefins using a photoredox catalyst under mild reaction conditions is presented. A variety of (Z)-alkenes can be prepared in the presence of visible light. A new reaction system allows an easy and efficient scale-up, as well as a continuous flow process in which the photocatalyst is immobilized in an ionic liquid and continuously recycled by simple phase separation. Catalytic (E)- to (Z)-isomerizations of olefins under mild conditions can be achieved by use of a photosensitizer and visible light. A new reaction system such as depicted allows an easy and efficient scale-up, as well as continuous flow processes in which the photocatalyst is immobilized in an ionic liquid and continuously recycled by phase separation.
Rhodium-catalyzed hydroformylation of alkynes employing a self-assembling ligand system
Agabekov, Vladislav,Seiche, Wolfgang,Breit, Bernhard
, p. 2418 - 2422 (2013/07/11)
Hydroformylation of alkynes is an underdeveloped atom-economic and redox-neutral method to prepare enals. Applying a new electron poor self-assembling ligand system provides the first general rhodium-catalyst for the chemo- and stereoselective hydroformylation of dialkyl- as well as diaryl-substituted alkynes to furnish enals in excellent chemo- and stereoselectivity.