том 49 издание 18 страницы 4327-4334

Asymmetric Friedel-Crafts/Michael Reaction of Indoles and Pyrroles with Coumarin-3-carbonylates

Тип публикацииJournal Article
Дата публикации2017-06-07
scimago Q2
wos Q2
БС2
SJR0.559
CiteScore4.6
Impact factor2.3
ISSN00397881, 1437210X
Catalysis
Organic Chemistry
Краткое описание

Asymmetric Friedel–Crafts reactions of indoles or pyrroles with coumarin-3-carboxylates catalyzed by Cu(OTf)2 complexes with chiral bis(oxazoline) ligands have been developed. The highest ee (up to 82%) was achieved for indole with a nitro derivative of coumarin-3-carboxylate­.

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ГОСТ |
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Beletskaya I., Beletskaya I. P. Asymmetric Friedel-Crafts/Michael Reaction of Indoles and Pyrroles with Coumarin-3-carbonylates // Synthesis. 2017. Vol. 49. No. 18. pp. 4327-4334.
ГОСТ со всеми авторами (до 50) Скопировать
Beletskaya I., Beletskaya I. P. Asymmetric Friedel-Crafts/Michael Reaction of Indoles and Pyrroles with Coumarin-3-carbonylates // Synthesis. 2017. Vol. 49. No. 18. pp. 4327-4334.
RIS |
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TY - JOUR
DO - 10.1055/s-0036-1589024
UR - https://doi.org/10.1055/s-0036-1589024
TI - Asymmetric Friedel-Crafts/Michael Reaction of Indoles and Pyrroles with Coumarin-3-carbonylates
T2 - Synthesis
AU - Beletskaya, Irina
AU - Beletskaya, Irina P.
PY - 2017
DA - 2017/06/07
PB - Georg Thieme Verlag KG
SP - 4327-4334
IS - 18
VL - 49
SN - 0039-7881
SN - 1437-210X
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2017_Beletskaya,
author = {Irina Beletskaya and Irina P. Beletskaya},
title = {Asymmetric Friedel-Crafts/Michael Reaction of Indoles and Pyrroles with Coumarin-3-carbonylates},
journal = {Synthesis},
year = {2017},
volume = {49},
publisher = {Georg Thieme Verlag KG},
month = {jun},
url = {https://doi.org/10.1055/s-0036-1589024},
number = {18},
pages = {4327--4334},
doi = {10.1055/s-0036-1589024}
}
MLA
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Beletskaya, Irina, and Irina P. Beletskaya. “Asymmetric Friedel-Crafts/Michael Reaction of Indoles and Pyrroles with Coumarin-3-carbonylates.” Synthesis, vol. 49, no. 18, Jun. 2017, pp. 4327-4334. https://doi.org/10.1055/s-0036-1589024.