1.
Beilstein J Org Chem
; 17: 1725-1726, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34367350
RESUMO
[This corrects the article DOI: 10.3762/bjoc.16.256.].
2.
Beilstein J Org Chem
; 16: 3069-3077, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33414854
RESUMO
The SF5Cl radical addition on unsaturated compounds was performed using an air-stable amine-borane complex as the radical initiator. This method showed to be complementary to the classic Et3B-mediated SF5Cl addition on alkenes and alkynes. A total of seven alkene and three alkyne derivatives were tested in the reaction, with yields ranging from 3% to 85%.
