Hypervalent Iodine‐Mediated Azidation Reactions
4
Department of Pharmacy Faculty of Pharmacy Aomori University 2-3-1 Kobata Aomori 030-0943 Japan
|
Publication type: Journal Article
Publication date: 2022-09-07
scimago Q2
wos Q2
SJR: 0.558
CiteScore: 4.3
Impact factor: 2.7
ISSN: 1434193X, 10990690
Organic Chemistry
Physical and Theoretical Chemistry
Abstract
Recently developed approaches to direct, one-step synthesis of various organic azides using hypervalent iodine reagents are summarized. Particularly useful azidating reagents are the stable azidobenziodoxoles that allow selective direct azidation of C−H single bonds or carbon-carbon double bonds under mild reaction conditions.
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32
Total citations:
32
Citations from 2024:
23
(74.19%)
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GOST
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Mironova I. A. et al. Hypervalent Iodine‐Mediated Azidation Reactions // European Journal of Organic Chemistry. 2022. Vol. 2022. No. 34.
GOST all authors (up to 50)
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Mironova I. A., Kirsch S., Zhdankin V. V., YOSHIMURA A., Yusubov M. S. Hypervalent Iodine‐Mediated Azidation Reactions // European Journal of Organic Chemistry. 2022. Vol. 2022. No. 34.
Cite this
RIS
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TY - JOUR
DO - 10.1002/ejoc.202200754
UR - https://doi.org/10.1002/ejoc.202200754
TI - Hypervalent Iodine‐Mediated Azidation Reactions
T2 - European Journal of Organic Chemistry
AU - Mironova, Irina A
AU - Kirsch, Stefan
AU - Zhdankin, Viktor V.
AU - YOSHIMURA, Akira
AU - Yusubov, Mekhman S.
PY - 2022
DA - 2022/09/07
PB - Wiley
IS - 34
VL - 2022
SN - 1434-193X
SN - 1099-0690
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2022_Mironova,
author = {Irina A Mironova and Stefan Kirsch and Viktor V. Zhdankin and Akira YOSHIMURA and Mekhman S. Yusubov},
title = {Hypervalent Iodine‐Mediated Azidation Reactions},
journal = {European Journal of Organic Chemistry},
year = {2022},
volume = {2022},
publisher = {Wiley},
month = {sep},
url = {https://doi.org/10.1002/ejoc.202200754},
number = {34},
doi = {10.1002/ejoc.202200754}
}