1+1>2!
Sluggish two-electron B-to-Cu transmetalation is overcome by two seamless single-electron events to unclock robust late-stage N-alkylation!
Excited to share my first corresponding author paper in @J_A_C_S !!🎉
@GestwickiLab
https://t.co/M1iNx6sqjI
🎉 Chuffed to see our JACS paper is among the most read articles this month!
See how a boron-mediated Ni/photoredox strategy for hydroalkylation of olefins enabled the access to quaternary carbons.
https://t.co/rf1HXDopsr
Congrats Team!
#Photoredox#Organoborons@BristolChem
Boron-Mediated Hydroalkylation of Unactivated Olefins: An Anti-Markovnikov Approach to Congested Carbon Center (@VarinderAggar11, @AggarwalLab): https://t.co/PUAFkNP315 (@J_A_C_S).
Radical Strategy to the Boron-to-Copper Transmetalation Problem: N-Alkylation with Alkylboronic Esters | Journal of the American Chemical Society @UCSF@TotalSyntheses https://t.co/kEobS70yql
1+1>2! Sluggish two-electron B-to-Cu transmetalation is overcome by two seamless single-electron events to unclock robust late-stage N-alkylation!
Excited to share my first corresponding author paper!
@GestwickiLab@UCSF@Boron_Chemistry
Radical Strategy to the Boron-to-Copper Transmetalation Problem: N-Alkylation with Alkylboronic Esters | Journal of the American Chemical Society @UCSF@TotalSyntheses https://t.co/kEobS70yql
1+1>2!
Sluggish two-electron B-to-Cu transmetalation is overcome by two seamless single-electron events to unclock robust late-stage N-alkylation!
Excited to share my first corresponding author paper in @J_A_C_S !!🎉
@GestwickiLab
https://t.co/M1iNx6sqjI