том 14 издание 5 номер публикации e202500104

Catalyst‐free One‐Pot Synthesis of Sulfonyl Fluorides from Triazenes via Multicomponent Reaction

Тип публикацииJournal Article
Дата публикации2025-03-20
scimago Q2
wos Q2
БС1
SJR0.542
CiteScore5.0
Impact factor2.7
ISSN21935807, 21935815
Краткое описание

Sulfonyl fluorides are valuable structures in organic chemistry and drug discovery. In this study, a novel metal‐ and catalyst‐free method for synthesizing sulfonyl fluorides from aryltriazenes was developed. This reaction employed a one‐pot, multi‐component approach using aryltriazenes, DABSO, and NFSI in the presence of TFA. Using this method, a variety of sulfonyl fluorides was readily synthesized from aryltriazenes in high yields. This approach features simple reaction conditions, broad functional group tolerance, and ease of operation, proving an efficient and practical strategy for the preparation of sulfonyl fluorides.

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Luu T. G., Kim H. Catalyst‐free One‐Pot Synthesis of Sulfonyl Fluorides from Triazenes via Multicomponent Reaction // Asian Journal of Organic Chemistry. 2025. Vol. 14. No. 5. e202500104
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Luu T. G., Kim H. Catalyst‐free One‐Pot Synthesis of Sulfonyl Fluorides from Triazenes via Multicomponent Reaction // Asian Journal of Organic Chemistry. 2025. Vol. 14. No. 5. e202500104
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TY - JOUR
DO - 10.1002/ajoc.202500104
UR - https://aces.onlinelibrary.wiley.com/doi/10.1002/ajoc.202500104
TI - Catalyst‐free One‐Pot Synthesis of Sulfonyl Fluorides from Triazenes via Multicomponent Reaction
T2 - Asian Journal of Organic Chemistry
AU - Luu, Truong Giang
AU - Kim, Hee-Kwon
PY - 2025
DA - 2025/03/20
PB - Wiley
IS - 5
VL - 14
SN - 2193-5807
SN - 2193-5815
ER -
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@article{2025_Luu,
author = {Truong Giang Luu and Hee-Kwon Kim},
title = {Catalyst‐free One‐Pot Synthesis of Sulfonyl Fluorides from Triazenes via Multicomponent Reaction},
journal = {Asian Journal of Organic Chemistry},
year = {2025},
volume = {14},
publisher = {Wiley},
month = {mar},
url = {https://aces.onlinelibrary.wiley.com/doi/10.1002/ajoc.202500104},
number = {5},
pages = {e202500104},
doi = {10.1002/ajoc.202500104}
}