@@ras6802 Thank you very much! Could you send me a CV (to synthesisworkshopvideos@gmail.com) or connect to me on LinkedIn (www.linkedin.com/in/matthew-horwitz-8a00861a4/) so I can see some of your work?
@@SynthesisWorkshopVideos Thank you for responding my message. I will follow you in LinkedIn. I am working on hypervalent iodine chemistry, but no publication yet.
Very professional, clear, and concise presentation.
I personally find that the tempo is little high. The rest is great!
Thanks - I'll try to find a better middleground in the future!
Can also reduce the playback speed 😁
I learned a lot and your inclusion of references/background is great. That's a pretty sick heterocycle synthesis.
I love how your videos fit as little "snacks" in my day! Please, keep on! (-:
Thank you, I will!
very well presented
Thank you very much - I appreciate the kind words!
Well presentation. Well explained. Keep upload videos like this.
Thank you very much! I will!
@@SynthesisWorkshopVideos I am also organic chemistry research scholar. If you need help, I would like to help in anyway.
@@ras6802 Thank you very much! Could you send me a CV (to synthesisworkshopvideos@gmail.com) or connect to me on LinkedIn (www.linkedin.com/in/matthew-horwitz-8a00861a4/) so I can see some of your work?
@@SynthesisWorkshopVideos Thank you for responding my message. I will follow you in LinkedIn. I am working on hypervalent iodine chemistry, but no publication yet.
Great work!
Btw Mislow & Siegel would be critical about terms as "prostereogenic center"
The pace is a bit fast for digesting new transformations.
Very instructive.
Thank you, I'm glad you enjoyed it!
Why before attaching DG, -Me is not a diastereotopic @2.20
Excuse me but we do we use silver triflate at the end coupling
Can you pronounce some of the things more clearly? at 2:07, i have no idea what you said. I'm assuming from the formula it's "oxalyl - chloride".
Yes, I'll work on that! That's correct, it's oxalyl chloride. Sorry about that!
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