In the michael addition of the vinyl group (20:12), what explains that it occured from the top face?

great video really interesting. it's great you split up the topics. as a practicing organic chemists i personally prefer the second half but you do a good job of making even me interested from the beginning, even though it's more biology than i can normally stomach.

well researched

waht

unsubbed for AI trash

The main reason why we try the synthesis ? The fun bro 😎

Sollux reference?

SUBTITLES!!!!! You should do one for Curcumin that actually treats cancer. <3

The synthesis route of Kalmanol was really interesting, particularly the ring closure of the core macrocycle. Great job!

At 18:39, why does the Gringard reagent not react with its own ketone group? I don't see why that ketone group would be any less reactive than the ketone of the other fragment, but I am only an undergrad.

Loved your exercises, I would love to do more of them !

Great content and in-depth explanations as always !

If it cures epileptics, why not use it in medicine?

One of my favorite accounts

This content is amazing, i love to dive deep. Of course i learn something and i like it a lot. Thanks for your work 🖖

good videos first of all

Thanks for watching! Hope you learned something new or liked it!

And thank you, for teaching us.

Interview dr. Mash

What courses/programs did you do in uni?

Excellent video and fascinating discussion, I really learnt a lot. But just to nitpick a bit, at 19:59 you forgot the other -Ar substituent on the structure at the bottom left