A dual palladium/photoredox-catalyzed regio- and enantioselective decarboxylative hydroaminoalkylation of allenes with amino acids is reported. This mild, redox-neutral, and atom-economic process allows access to a range of protected vinyl 1,2-amino ethers in good yields with high levels of branched and enantioselectivity, when alkoxyallenes were employed. Conversely, with alkyl- and aryl-substituted terminal allenes as the substrates, a linear-selective decarboxylative hydroaminoalkylation of allenes is realized in high regio- and E / Z selectivities with a Pd/ rac -BINAP catalytic system.
No takes yet. Share an insight, caveat, or question.
Zheng et al. (2021) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: