том 134 издание 4 номер публикации 121

Efficient synthesis of 3-aminocarbazoles from N-sulfonyl-1,2,3-triazoles and 2-alkenylindole

Тип публикацииJournal Article
Дата публикации2022-12-13
scimago Q3
wos Q3
white level БС2
SJR0.334
CiteScore3
Impact factor2
ISSN09743626, 09737103, 02534134
General Chemistry
Краткое описание
An efficient two-step protocol for the synthesis of 3-aminocarbazoles has been accomplished from N-sulfonyl-1,2,3-triazoles and 2-alkenylindoles. The present method tolerates various functional groups and allows the synthesis of diverse 3-aminocarbazoles in good to excellent yield. Furthermore, the developed method was successfully applied in the synthesis of indolocarbazole derivative through an oxidative amination. An efficient two-step protocol for synthesizing 3-aminocarbazoles has been accomplished from N-sulfonyl-1,2,3-triazoles and 2-alkenylindoles.
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Rajasekar S., Ramachandran K., Anbarasan P. Efficient synthesis of 3-aminocarbazoles from N-sulfonyl-1,2,3-triazoles and 2-alkenylindole // Journal of Chemical Sciences. 2022. Vol. 134. No. 4. 121
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Rajasekar S., Ramachandran K., Anbarasan P. Efficient synthesis of 3-aminocarbazoles from N-sulfonyl-1,2,3-triazoles and 2-alkenylindole // Journal of Chemical Sciences. 2022. Vol. 134. No. 4. 121
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TY - JOUR
DO - 10.1007/s12039-022-02111-8
UR - https://doi.org/10.1007/s12039-022-02111-8
TI - Efficient synthesis of 3-aminocarbazoles from N-sulfonyl-1,2,3-triazoles and 2-alkenylindole
T2 - Journal of Chemical Sciences
AU - Rajasekar, Shanmugam
AU - Ramachandran, Kuppan
AU - Anbarasan, Pazhamalai
PY - 2022
DA - 2022/12/13
PB - Springer Nature
IS - 4
VL - 134
SN - 0974-3626
SN - 0973-7103
SN - 0253-4134
ER -
BibTex
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@article{2022_Rajasekar,
author = {Shanmugam Rajasekar and Kuppan Ramachandran and Pazhamalai Anbarasan},
title = {Efficient synthesis of 3-aminocarbazoles from N-sulfonyl-1,2,3-triazoles and 2-alkenylindole},
journal = {Journal of Chemical Sciences},
year = {2022},
volume = {134},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007/s12039-022-02111-8},
number = {4},
pages = {121},
doi = {10.1007/s12039-022-02111-8}
}
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