1999Chinese Journal of Organic ChemistryRequires access

Synthesis of Chlorin e_6 - 6 - amide Derivatives

De Xu

Open publisher page 3 citations

Abstract

A mixture of pheophorbide a and pyropheophorbide a was prepared by acid degradation of silkworm excrement crude chlorophylls. Pheophorbide a obtained reacted directly with amines through the cleavage of its cyclopentanone ring V without separation. 11 chlorin e6 - 6 - amides were thus synthesized.

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A mixture of pheophorbide a and pyropheophorbide a was prepared by acid degradation of silkworm excrement crude chlorophylls. Pheophorbide a obtained reacted directly with amines through the cleavage of its cyclopentanone ring V without separation. 11 chlorin e6 - 6 - amides were thus synthesized.

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Available abstract

A mixture of pheophorbide a and pyropheophorbide a was prepared by acid degradation of silkworm excrement crude chlorophylls. Pheophorbide a obtained reacted directly with amines through the cleavage of its cyclopentanone ring V without separation. 11 chlorin e6 - 6 - amides were thus synthesized.

Key concepts: Pheophorbide A, Chlorin, Chemistry, Cyclopentanone, Amide, Ring (chemistry), Cleavage (geology), Organic chemistry

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