1.
ACS Omega
; 5(36): 22914-22925, 2020 Sep 15.
Article
in English
| MEDLINE
| ID: mdl-32954140
ABSTRACT
A pathway to a range of diverse heterocycles was developed using a nucleophilic cyclization strategy. Lactams and ene-imines are accessed in a few steps from a common precursor, and these moieties are further elaborated to directly provide pyrroles or pyridines with extended conjugation. Reaction conditions are mild, and a broad range of structural types are available within a few steps.