Standard

N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes. / Miltsov, Sergey; Yakimansky, Alexander; Mitroshin, Alexander; Gurzhiy, Vladislav; Alonso-Chamarro, Julian; Puyol, Mar.

в: Tetrahedron, Том 140, 133485, 01.06.2023.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Miltsov, S, Yakimansky, A, Mitroshin, A, Gurzhiy, V, Alonso-Chamarro, J & Puyol, M 2023, 'N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes', Tetrahedron, Том. 140, 133485. https://doi.org/10.1016/j.tet.2023.133485

APA

Miltsov, S., Yakimansky, A., Mitroshin, A., Gurzhiy, V., Alonso-Chamarro, J., & Puyol, M. (2023). N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes. Tetrahedron, 140, [133485]. https://doi.org/10.1016/j.tet.2023.133485

Vancouver

Miltsov S, Yakimansky A, Mitroshin A, Gurzhiy V, Alonso-Chamarro J, Puyol M. N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes. Tetrahedron. 2023 Июнь 1;140. 133485. https://doi.org/10.1016/j.tet.2023.133485

Author

Miltsov, Sergey ; Yakimansky, Alexander ; Mitroshin, Alexander ; Gurzhiy, Vladislav ; Alonso-Chamarro, Julian ; Puyol, Mar. / N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes. в: Tetrahedron. 2023 ; Том 140.

BibTeX

@article{9c7c66e2130e447b9fbec7f09e2e742a,
title = "N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes",
abstract = "The reaction of indodicarbocyanine dyes with N-iodosuccinimide produces dimeric molecules together with the corresponding meso-iodinated dyes depending on the aryl substitution of the dyes and reaction conditions. Iodinated dyes are more reactive in BF3-catalized dimerization than brominated analogues. Reaction of N-iodosuccinimide with N,N′-connected dimeric pentamethines gave rise to macrocyclic dyes with 16- and 20-membered cycles.",
keywords = "Cyanine dyes, Cyclization, Dimerization, N-iodosuccinimide",
author = "Sergey Miltsov and Alexander Yakimansky and Alexander Mitroshin and Vladislav Gurzhiy and Julian Alonso-Chamarro and Mar Puyol",
year = "2023",
month = jun,
day = "1",
doi = "10.1016/j.tet.2023.133485",
language = "English",
volume = "140",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - N-Iodosuccinimide-mediated dimerization and macrocyclization of indodicarbocyanine dyes

AU - Miltsov, Sergey

AU - Yakimansky, Alexander

AU - Mitroshin, Alexander

AU - Gurzhiy, Vladislav

AU - Alonso-Chamarro, Julian

AU - Puyol, Mar

PY - 2023/6/1

Y1 - 2023/6/1

N2 - The reaction of indodicarbocyanine dyes with N-iodosuccinimide produces dimeric molecules together with the corresponding meso-iodinated dyes depending on the aryl substitution of the dyes and reaction conditions. Iodinated dyes are more reactive in BF3-catalized dimerization than brominated analogues. Reaction of N-iodosuccinimide with N,N′-connected dimeric pentamethines gave rise to macrocyclic dyes with 16- and 20-membered cycles.

AB - The reaction of indodicarbocyanine dyes with N-iodosuccinimide produces dimeric molecules together with the corresponding meso-iodinated dyes depending on the aryl substitution of the dyes and reaction conditions. Iodinated dyes are more reactive in BF3-catalized dimerization than brominated analogues. Reaction of N-iodosuccinimide with N,N′-connected dimeric pentamethines gave rise to macrocyclic dyes with 16- and 20-membered cycles.

KW - Cyanine dyes

KW - Cyclization

KW - Dimerization

KW - N-iodosuccinimide

UR - https://www.mendeley.com/catalogue/1efb1f94-def9-3132-b5e8-292b778cb999/

U2 - 10.1016/j.tet.2023.133485

DO - 10.1016/j.tet.2023.133485

M3 - Article

VL - 140

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

M1 - 133485

ER -

ID: 108185783