https://www.pieberlab.com/
-Couples tough nucleophiles (yes, 3° alcohols!)
-Couples electron-rich aryl bromides
-Doesn't need a PC
-Runs on 100 ppm Ni
-Delivers on drug syntheses and late-stage modifications
Now on @chemrxiv.org: tinyurl.com/3ss6x24j
-Couples tough nucleophiles (yes, 3° alcohols!)
-Couples electron-rich aryl bromides
-Doesn't need a PC
-Runs on 100 ppm Ni
-Delivers on drug syntheses and late-stage modifications
Now on @chemrxiv.org: tinyurl.com/3ss6x24j
-Couples tough nucleophiles (yes, 3° alcohols!)
-Couples electron-rich aryl bromides
-Doesn't need a PC
-Runs on 100 ppm Ni
-Delivers on drug syntheses and late-stage modifications
Now on @chemrxiv.org: tinyurl.com/3ss6x24j
Wishing you all the best for whatever comes next, Lucia. We’re so proud of you—and can’t wait to see where your next chapter takes you! 💫
Wishing you all the best for whatever comes next, Lucia. We’re so proud of you—and can’t wait to see where your next chapter takes you! 💫
For all details, see: photoexcite.ist.ac.at
For all details, see: photoexcite.ist.ac.at
Check out our 🆕 photoactive nickel catalyst that makes C-C and C-heteroatom bonds without an exogeneous photocatalyst. This was a mechanistically fascinating study that came out today @jacs.acspublications.org
pubs.acs.org/doi/10.1021/...
Congrats to the team!
Check out our 🆕 photoactive nickel catalyst that makes C-C and C-heteroatom bonds without an exogeneous photocatalyst. This was a mechanistically fascinating study that came out today @jacs.acspublications.org
pubs.acs.org/doi/10.1021/...
Congrats to the team!