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 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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. |
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ISSN: | 0959-9436 1364-557X |
DOI: | 10.1070/MC2003v013n04ABEH001735 |