CBS Reduction, Enantioselective Catalysis - Organic Chemistry, Reaction Mechanism

[@ProfessorWaltherKotz]

This is content of highest quality, thanks!

[@CasualChemistry]

Many thanks for the feedback 🙂 Very much appreciated

[@AlphaNumeric123]

Wow impressive. Great video as always!

[@CasualChemistry]

Thanks for the feedback 🙂 Very much appreciated

[@shaunkelly7223]

Appreciate your work! Looking forward for your upcoming vids!

[@CasualChemistry]

Many thanks for the feedback 😃 More on the way soon once I get through a chaotic week at work.

[@wiktormazur7027]

I love your videos that's the kind of chemistry that i really enjoy.

[@CasualChemistry]

Thanks for the feedback - glad you’re enjoying the videos 😀 This is becoming a really rewarding hobby for me so there are more to come. I’m going to experiment with some other connected areas as I’m a fan of stereochemistry in organic synthesis. It was the thing that really clicked with the subject for me.

[@ruthpay]

Such a clear explanation, thank you!

[@CasualChemistry]

Thanks for the feedback 🙂 Glad you found the video helpful

[@iamahero1635]

The oxazaborolidine catalyst is relatively cheap since it's synthesized from proline ! I didn't know that. Thanks.

[@CasualChemistry]

That proline gets everywhere in this field. I use trying to spot amino acids as a way of remembering the catalyst structures.

[@9vp100]

Please sir, can u do a video in alpine boran model’s ( enatioselective reduction of ketone and aldehayde ) ??

[@CasualChemistry]

I have a plan to do a stoichiometric reducing agent video at some point that would include things like this. In practice though nowadays, the CBS reduction superseded things like this and is the superior one to do in the lab for the same sort of substrates in my opinion.

[@nihalkhatiwoda6961]

Sleek

[@CasualChemistry]

Thanks - glad you enjoyed the video 🙂

[@nihalkhatiwoda6961]

@@CasualChemistry please keep making videos.