Synthesis of diethyl (aryl)(4-oxopiperidin-1-yl)methylphosphonates
Publication type: Journal Article
Publication date: 2015-05-01
scimago Q3
wos Q3
SJR: 0.305
CiteScore: 3.0
Impact factor: 1.7
ISSN: 09599436, 1364551X
General Chemistry
Abstract
The Kabachnik–Fields reaction of 4-piperidone hydrochloride monohydrate, an aromatic aldehyde and triethyl phosphite in the presence of triethylamine and magnesium perchlorate affords diethyl (aryl)(4-oxopiperidin-1-yl)methylphosphonates in moderate yields.
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Makarov M. V., Skvortsov E. A., Brel V. K. Synthesis of diethyl (aryl)(4-oxopiperidin-1-yl)methylphosphonates // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 232-233.
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Makarov M. V., Skvortsov E. A., Brel V. K. Synthesis of diethyl (aryl)(4-oxopiperidin-1-yl)methylphosphonates // Mendeleev Communications. 2015. Vol. 25. No. 3. pp. 232-233.
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TY - JOUR
DO - 10.1016/j.mencom.2015.05.026
UR - https://doi.org/10.1016/j.mencom.2015.05.026
TI - Synthesis of diethyl (aryl)(4-oxopiperidin-1-yl)methylphosphonates
T2 - Mendeleev Communications
AU - Makarov, Michael V.
AU - Skvortsov, Evgenii A
AU - Brel, Valery K.
PY - 2015
DA - 2015/05/01
PB - OOO Zhurnal "Mendeleevskie Soobshcheniya"
SP - 232-233
IS - 3
VL - 25
SN - 0959-9436
SN - 1364-551X
ER -
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@article{2015_Makarov,
author = {Michael V. Makarov and Evgenii A Skvortsov and Valery K. Brel},
title = {Synthesis of diethyl (aryl)(4-oxopiperidin-1-yl)methylphosphonates},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {OOO Zhurnal "Mendeleevskie Soobshcheniya"},
month = {may},
url = {https://doi.org/10.1016/j.mencom.2015.05.026},
number = {3},
pages = {232--233},
doi = {10.1016/j.mencom.2015.05.026}
}
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MLA
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Makarov, Michael V., et al. “Synthesis of diethyl (aryl)(4-oxopiperidin-1-yl)methylphosphonates.” Mendeleev Communications, vol. 25, no. 3, May. 2015, pp. 232-233. https://doi.org/10.1016/j.mencom.2015.05.026.