NOVEL CYCLOIMIDES IN THE CHLOROPHYLL a SERIES

A.F. Mironov*^a, M.A. Grin^a, S.A. Nochovny^a, Ph.V. Toukach^b

^aM.V. Lomonosov Academy of Fine Chemical Technology, Moscow, Russia
^bN.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia

Mendeleev's Communications, 2003, v. 13(4), p.156-158

DOI: 10.1070/MC2003v013n04ABEH001735

The reaction of hydrazine hydrate with purpurin 18 was studied. The resulting monohydrazide readily reacts with the second carboxy group on acidification to give a six-membered chlorin p₆ N-aminocycloimide with the reduction of the vinyl group to ethyl.

Publications: Rest

Home : Science