![organic chemistry - Why does the reduction of a Weinreb amide give an aldehyde instead of an amine? - Chemistry Stack Exchange organic chemistry - Why does the reduction of a Weinreb amide give an aldehyde instead of an amine? - Chemistry Stack Exchange](https://i.stack.imgur.com/Dfvf5.png)
organic chemistry - Why does the reduction of a Weinreb amide give an aldehyde instead of an amine? - Chemistry Stack Exchange
![Reactions of a novel modified Red-Al reducing agent with selected organic compounds containing representative functional groups and chemoselective reduction - ScienceDirect Reactions of a novel modified Red-Al reducing agent with selected organic compounds containing representative functional groups and chemoselective reduction - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403916306438-fx1.jpg)
Reactions of a novel modified Red-Al reducing agent with selected organic compounds containing representative functional groups and chemoselective reduction - ScienceDirect
![Cp 2 TiCl 2 -catalyzed cis -hydroalumination of propargylic amines with Red- Al: stereoselective synthesis of Z -configured allylic amines - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC00950B Cp 2 TiCl 2 -catalyzed cis -hydroalumination of propargylic amines with Red- Al: stereoselective synthesis of Z -configured allylic amines - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC00950B](https://pubs.rsc.org/image/article/2015/CC/c5cc00950b/c5cc00950b-s1_hi-res.gif)
Cp 2 TiCl 2 -catalyzed cis -hydroalumination of propargylic amines with Red- Al: stereoselective synthesis of Z -configured allylic amines - Chemical Communications (RSC Publishing) DOI:10.1039/C5CC00950B
![organic chemistry - Why does the reduction of a Weinreb amide give an aldehyde instead of an amine? - Chemistry Stack Exchange organic chemistry - Why does the reduction of a Weinreb amide give an aldehyde instead of an amine? - Chemistry Stack Exchange](https://i.stack.imgur.com/yc0Aj.png)