Thank you so much! I'm thrilled to hear you enjoy the videos. Your support means a lot, and I can't wait to share more content with you in the future! 😊🎥✨
Thank you so much for the kind words! I'm thrilled you enjoy the videos. Yes, I use blender to create 3D space. I believe that 3D visualization is essential for understanding organic chemistry.🎥🔬
@@Chemicatoralso ummm the mitsunobu reaction should be a steglich esterification instead since mitsunobu uses triphenylphosphine and no stereo chemical inversion
One of the interesting features of the mitsunobu reaction is the ability to invert the stereochemistry of the alcohol. Check out the reference of the video to gain a deeper understanding.
wow, your videos are absolutely stunning!! love it! looking forward for your future uploads!
Thank you so much! I'm thrilled to hear you enjoy the videos. Your support means a lot, and I can't wait to share more content with you in the future! 😊🎥✨
Thia was a pleasure to watch. Nice job!
Thank you! I'm so glad you enjoyed it. Your feedback makes all the hard work worthwhile! 😊🎉
I love your videos...well done!!! Do you use blender/molecular nodes? Very insightful and visually quite appealing. Thank you!!!
Thank you so much for the kind words! I'm thrilled you enjoy the videos. Yes, I use blender to create 3D space. I believe that 3D visualization is essential for understanding organic chemistry.🎥🔬
Think you missed the extra O for the TEMPO appended to the substrate past 5:45 something
And there’s an extra carbon for the CHCl2 step
Thanks for pointing that out! I appreciate your attention to detail. Your feedback is super helpful! 😊🔬
@@Chemicatoralso ummm the mitsunobu reaction should be a steglich esterification instead since mitsunobu uses triphenylphosphine and no stereo chemical inversion
One of the interesting features of the mitsunobu reaction is the ability to invert the stereochemistry of the alcohol.
Check out the reference of the video to gain a deeper understanding.