| Literature DB >> 31063384 |
Pavel A Sakharov1, Nikolai V Rostovskii1, Alexander F Khlebnikov1, Taras L Panikorovskii1,2, Mikhail S Novikov1.
Abstract
A method of furo-annulation of 4-hydroxy-2-oxoquinoline-3-carboxylates with 3-arylazirines under Cu(II) catalysis was developed to synthesize a variety of 2,3-dihydrofuro[3,2- c]quinolones bearing a carbamate group at the C2 position. The reaction involves an azirine ring opening across the N-C2 bond and formation of a dihydrofuran ring with the inclusion of two azirine carbon atoms, accompanied by a shift of the ester group to the nitrogen. The discovered reaction is the first example of the use of 2 H-azirines for furo-annulation.Entities:
Year: 2019 PMID: 31063384 DOI: 10.1021/acs.orglett.9b01043
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005