Mingoia, Francesco published the artcile< Reactivity of 5-(3-azidophenyl)-1-(1H-pyrrol-3-yl)pyrroles in TFMSA. A route for new ring systems as DNA-interactive agents>, Formula: C7H10N2O2, the main research area is azidophenyl pyrrolylpyrrole preparation cyclization; dipyrroloisoquinoline preparation DNA interactive agent.
Acid catalyzed decomposition of 5-(3-azidophenyl)-1-(1H-pyrrol-3-yl)pyrroles did not afford the expected dipyrrolo[2,1-a:3,4-c]isoquinoline derivatives, but the planar dipyrrolo[2,1-a:3,2-c]isoquinoline derivatives and related non planar derivatives H-dipyrrolo[2,1-a:3,2-c]isoquinoline derivatives In strong acid media (trifluoromethanesulfonic acid) the α-(1-pyrrol-3-yl) position even if blocked, was more prone to undergo cyclization with respect to the free β one. Despite the steric hindrance, these compounds were obtained in moderate to good overall yields, depending on the nature and position of the substituents on the 1-(1H-pyrrolyl) moiety.
Tetrahedron published new progress about DNA Role: MSC (Miscellaneous). 252932-48-2 belongs to class esters-buliding-blocks, and the molecular formula is C7H10N2O2, Formula: C7H10N2O2.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics