том 2022 издание 34

Hypervalent Iodine‐Mediated Azidation Reactions

Тип публикацииJournal Article
Дата публикации2022-09-07
scimago Q2
wos Q2
БС2
SJR0.558
CiteScore4.3
Impact factor2.7
ISSN1434193X, 10990690
Organic Chemistry
Physical and Theoretical Chemistry
Краткое описание
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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ГОСТ |
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Mironova I. A. et al. Hypervalent Iodine‐Mediated Azidation Reactions // European Journal of Organic Chemistry. 2022. Vol. 2022. No. 34.
ГОСТ со всеми авторами (до 50) Скопировать
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.
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 -
BibTex
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BibTex (до 50 авторов) Скопировать
@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}
}