Novel cycloimides in the chlorophyll a series

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 p 6 N-aminocycloimide with the reduction of the vinyl group to ethyl.

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Veröffentlicht in:Mendeleev communications 2003, Vol.13 (4), p.156-157
Hauptverfasser: Mironov, Andrei F., Grin, Michael A., Nochovny, Sergei A., Toukach, Philipp V.
Format: Artikel
Sprache:eng
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Zusammenfassung: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 p 6 N-aminocycloimide with the reduction of the vinyl group to ethyl.
ISSN:0959-9436
1364-557X
DOI:10.1070/MC2003v013n04ABEH001735