Mendeleev Communications
,  том 25 ,  издание 2 ,  страницы 126-128

Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids

Тип публикации: Journal Article
Дата публикации: 2015-03-01
scimago Q3
wos Q3
БС1
SJR: 0.305
CiteScore: 3.0
Impact factor: 1.7
ISSN: 09599436, 1364551X
General Chemistry
Краткое описание
The Chapman rearrangement of aryl N -arylbenzimidates to tertiary acyclic amides is accelerated in ionic liquids and proceeds at lower temperatures as 120–190°C.
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Epishina M. A. et al. Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids // Mendeleev Communications. 2015. Vol. 25. No. 2. pp. 126-128.
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Epishina M. A., Kulikov A., Ignat’ev N. V., Schulte M., Makhova N. N. Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids // Mendeleev Communications. 2015. Vol. 25. No. 2. pp. 126-128.
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TY - JOUR
DO - 10.1016/j.mencom.2015.03.016
UR - https://doi.org/10.1016/j.mencom.2015.03.016
TI - Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids
T2 - Mendeleev Communications
AU - Epishina, Margarita A.
AU - Kulikov, Alexander
AU - Ignat’ev, Nikolai V.
AU - Schulte, Michael
AU - Makhova, Nina N.
PY - 2015
DA - 2015/03/01
PB - OOO Zhurnal "Mendeleevskie Soobshcheniya"
SP - 126-128
IS - 2
VL - 25
SN - 0959-9436
SN - 1364-551X
ER -
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@article{2015_Epishina,
author = {Margarita A. Epishina and Alexander Kulikov and Nikolai V. Ignat’ev and Michael Schulte and Nina N. Makhova},
title = {Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {OOO Zhurnal "Mendeleevskie Soobshcheniya"},
month = {mar},
url = {https://doi.org/10.1016/j.mencom.2015.03.016},
number = {2},
pages = {126--128},
doi = {10.1016/j.mencom.2015.03.016}
}
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Epishina, Margarita A., et al. “Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids.” Mendeleev Communications, vol. 25, no. 2, Mar. 2015, pp. 126-128. https://doi.org/10.1016/j.mencom.2015.03.016.