Asymmetric synthesis of bicyclic dihydropyrans via organocatalytic inverse-electron-demand oxo-Diels–Alder reactions of enolizable aliphatic aldehydes - Chemical Communications (RSC Publishing)
![Figure 2. Scheme of the Ruhrchemie/ Rhône-Poulenc oxo process. a) reaction scheme and structure of the rhodium catalyst. b) Formation of biphasic liquid mixture that is split in a separator to obtain Figure 2. Scheme of the Ruhrchemie/ Rhône-Poulenc oxo process. a) reaction scheme and structure of the rhodium catalyst. b) Formation of biphasic liquid mixture that is split in a separator to obtain](http://pubs.sciepub.com/wjce/7/2/15/bigimage/fig2.png)
Figure 2. Scheme of the Ruhrchemie/ Rhône-Poulenc oxo process. a) reaction scheme and structure of the rhodium catalyst. b) Formation of biphasic liquid mixture that is split in a separator to obtain
Explain in detail the mechanism (along with the role of catalyst) of Wacker process and oxo process for the synthesis of aldehydes and ketones
![The incorrect statement regarding oxo process for synthesis of an aldehyde is | 12 | ALDEHYDES,... - YouTube The incorrect statement regarding oxo process for synthesis of an aldehyde is | 12 | ALDEHYDES,... - YouTube](https://i.ytimg.com/vi/SJQyK37NlRg/maxresdefault.jpg?sqp=-oaymwEmCIAKENAF8quKqQMa8AEB-AH-CYAC0AWKAgwIABABGD4gZShCMA8=&rs=AOn4CLAkMrogsxfhsobHuSno68ghtVKKcw)