β-Keto ester aminolysis of pheophorbide a methyl ester: a facile route for asymmetric chlorin ring substitution
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Chemistry of Chlorophylls in Chlorophylls;Hynninen,1991
2. Chlorophylls and bacteriochlorophylls;Senge,2006
3. Teilsynthese des Chlorophyllids a
4. Reaction of chlorophylls a and b with amines. Isocyclic ring rupture and formation of substituted chlorin-6-amides
5. Transesterification of the α-keto ester in methyl pheophorbide-a
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1. Synthesis of Red‐Light‐Responsive Pheophorbide‐a Tryptamine Conjugated Photosensitizers for Photodynamic Therapy;ChemMedChem;2022-11-14
2. C–O, C–S, C–N, and C–C Bond Formation at the Periphery of the Macrocycle during Chemical Modification of Phytochlorins: Key Methods and Synthetic Applications;Russian Journal of General Chemistry;2019-12
3. Syntheses and cellular investigations of di-aspartate and aspartate-lysine chlorin e6 conjugates;Organic & Biomolecular Chemistry;2016
4. C132-Methylation of methyl pheophorbide a and stereoselective preparation of methyl (132R)-methylpyropheophorbide a;Tetrahedron Letters;2014-06
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