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Inverse electron demand Diels–Alder reaction as a novel method for functionalization of natural chlorins

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Suvorov N. V. et al. Inverse electron demand Diels–Alder reaction as a novel method for functionalization of natural chlorins // Mendeleev Communications. 2019. Vol. 29. No. 2. pp. 206-208.
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Suvorov N. V., Cheskov D. A., Mironov A. F., Grin M. A. Inverse electron demand Diels–Alder reaction as a novel method for functionalization of natural chlorins // Mendeleev Communications. 2019. Vol. 29. No. 2. pp. 206-208.
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TY - JOUR
DO - 10.1016/j.mencom.2019.03.031
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.03.031
TI - Inverse electron demand Diels–Alder reaction as a novel method for functionalization of natural chlorins
T2 - Mendeleev Communications
AU - Suvorov, Nikita Vladimirovich
AU - Cheskov, Dmitry A
AU - Mironov, Andrey Fedorovich
AU - Grin, Mikhail Alexandrovich
PY - 2019
DA - 2019/03/01
PB - Mendeleev Communications
SP - 206-208
IS - 2
VL - 29
ER -
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@article{2019_Suvorov,
author = {Nikita Vladimirovich Suvorov and Dmitry A Cheskov and Andrey Fedorovich Mironov and Mikhail Alexandrovich Grin},
title = {Inverse electron demand Diels–Alder reaction as a novel method for functionalization of natural chlorins},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.03.031},
number = {2},
pages = {206--208},
doi = {10.1016/j.mencom.2019.03.031}
}
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Suvorov, Nikita Vladimirovich, et al. “Inverse electron demand Diels–Alder reaction as a novel method for functionalization of natural chlorins.” Mendeleev Communications, vol. 29, no. 2, Mar. 2019, pp. 206-208. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.03.031.

Abstract

The addition of 3-aryl-1,2,4,5-tetrazines at the vinyl group of chlorin e6 trimethyl ester affords the corresponding pyridazine–porphyrin conjugates. The study of spectral properties of the obtained compounds revealed insignificant changes in the absorbance and fluorescence spectra as compared to those of chlorin.

References

1.
Gushchina O.I., Gramma V.A., Larkina E.A., Mironov A.F.
Mendeleev Communications, 2017
2.
Chlorins: Natural Sources, Synthetic Developments and Main Applications
Oliveira K., Momo P., Assis F., Ferreira M., Brocksom T.
Current Organic Synthesis, 2014
4.
10.1016/j.mencom.2019.03.031_bib0020
Gorshkova
Tonkie Khimicheskie Tekhnologii, 2018
5.
Syntheses and cellular investigations of 17(3)-, 15(2)-, and 13(1)-amino acid derivatives of chlorin e(6).
Jinadasa R.G., Hu X., Vicente M.G., Smith K.M.
Journal of Medicinal Chemistry, 2011
6.
Syntheses and PDT activity of new mono- and di-conjugated derivatives of chlorin e6.
Chen H., Humble S.W., Jinadasa R.G., Zhou Z., Nguyen A.L., Vicente M.G., Smith K.M.
Journal of Porphyrins and Phthalocyanines, 2017
7.
Synthesis of PSMA-targeted 131- and 152-substituted chlorin e6 derivatives and their biological properties
Suvorov N.V., Machulkin A.E., Ivanova A.V., Popkov A.M., Bondareva E.A., Plotnikova E.A., Yakubovskaya R.I., Majouga A.G., Mironov A.F., Grin M.A.
Journal of Porphyrins and Phthalocyanines, 2018
9.
Novel Synthetic Routes to 8-Vinyl Chlorophyll Derivatives
Gerlach B., Brantley S.E., Smith K.M.
Journal of Organic Chemistry, 1998
10.
Lebedeva V.S., Karmova F.M., Toukach F.V., Mironov A.F.
Mendeleev Communications, 2015
11.
Lonin I.S., Grin M.A., Lakhina A.A., Mironov A.F.
Mendeleev Communications, 2012
13.
The growing impact of click chemistry on drug discovery
Kolb H.C., Sharpless K.B.
Drug Discovery Today, 2003
14.
Reactions of Tetrazines with Unsaturated Compounds. A New Synthesis of Pyridazines
Carboni R.A., Lindsey R.V.
Journal of the American Chemical Society, 1959
15.
Inverse electron demand Diels-Alder reactions in chemical biology.
Oliveira B.L., Guo Z., Bernardes G.J.
Chemical Society Reviews, 2017
16.
Synthesis and Evaluation of a Series of 1,2,4,5-Tetrazines for Bioorthogonal Conjugation
Karver M.R., Weissleder R., Hilderbrand S.A.
Bioconjugate Chemistry, 2011