Abstract:
The synthesis of N-substituted cycloimide chlorin p6 with a D-galactose residue by simultaneous glycosylation of the main macrocycle followed by replacement of oxygen in the additional ring of purpurin 18 by nitrogen has been carried out to give a rigid spacer section in the form of a six-membered cycloimide.
Document Type:
Article
Language: English
Citation:
V. S. Lebedeva, R. D. Ruziev, A. V. Popov, Yu. L. Sebyakin, A. F. Mironov, “Synthesis of glycoconjugated chlorin p6 cycloimide”, Mendeleev Commun., 17:4 (2007), 212–213
Linking options:
https://www.mathnet.ru/eng/mendc3432
https://www.mathnet.ru/eng/mendc/v17/i4/p212
This publication is cited in the following 5 articles:
M. A. Grin, N. V. Suvorov, A. F. Mironov, “Natural chlorins as a promising platform for creating targeted theranostics in oncology”, Mendeleev Commun., 30:4 (2020), 406–418
D. V. Belykh, “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”, Russ J Gen Chem, 89:12 (2019), 2604
A. F. Mironov, “Chemical Transformations of Chlorophyll a and Possible Areas for Application of Its Derivatives”, Russ J Gen Chem, 89:9 (2019), 1952
Shivaji A. Thadke, Mahesh Neralkar, Srinivas Hotha, “Facile synthesis of aminooxy glycosides by gold(III)-catalyzed glycosidation”, Carbohydrate Research, 430 (2016), 16
David J. Harvey, “Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2007–2008”, Mass Spectrometry Reviews, 31:2 (2012), 183
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