Home / Publications / Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group

Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group

Liliya Il'gizovna Vagapova 1
Liliya Il'gizovna Vagapova
, 
Julia Konstantinovna Voronina 1
Julia Konstantinovna Voronina
, 
Victor Vasil'evich Syakaev 1
Victor Vasil'evich Syakaev
, 
Alexander Romanovich Burilov 1
Alexander Romanovich Burilov
,  , 
Michael Arkad'evich Pudovik 1
Michael Arkad'evich Pudovik
10.1016/j.mencom.2018.07.019
Published 2018-06-29
Communication , Volume 28, Issue 4, 398-400
6
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Vagapova L. I. et al. Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group // Mendeleev Communications. 2018. Vol. 28. No. 4. pp. 398-400.
GOST all authors (up to 50) Copy
Vagapova L. I., Voronina J. K., Syakaev V. V., Burilov A. R., Garyfzyanov A. R., Pudovik M. A. Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group // Mendeleev Communications. 2018. Vol. 28. No. 4. pp. 398-400.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2018.07.019
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.07.019
TI - Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group
T2 - Mendeleev Communications
AU - Vagapova, Liliya Il'gizovna
AU - Voronina, Julia Konstantinovna
AU - Syakaev, Victor Vasil'evich
AU - Burilov, Alexander Romanovich
AU - Garyfzyanov, Airat Rizvanovich
AU - Pudovik, Michael Arkad'evich
PY - 2018
DA - 2018/06/29
PB - Mendeleev Communications
SP - 398-400
IS - 4
VL - 28
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2018_Vagapova,
author = {Liliya Il'gizovna Vagapova and Julia Konstantinovna Voronina and Victor Vasil'evich Syakaev and Alexander Romanovich Burilov and Airat Rizvanovich Garyfzyanov and Michael Arkad'evich Pudovik},
title = {Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group},
journal = {Mendeleev Communications},
year = {2018},
volume = {28},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.07.019},
number = {4},
pages = {398--400},
doi = {10.1016/j.mencom.2018.07.019}
}
MLA
Cite this
MLA Copy
Vagapova, Liliya Il'gizovna, et al. “Synthesis and structure of new 2-aryl-substituted pyrrolidines containing phosphine oxide group.” Mendeleev Communications, vol. 28, no. 4, Jun. 2018, pp. 398-400. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.07.019.

Abstract

2-Aryl-substituted pyrrolidines containing phosphine oxide group have been obtained by the reaction of P-(4,4-diethoxybutylaminomethyl)-P,P-di-p-tolylphosphine oxide with polyatomic phenols.

References

2.
In vitro and In vivo Molecular Evidence for Better Therapeutic Efficacy of ABT-627 and Taxotere Combination in Prostate Cancer
Banerjee S., Hussain M., Wang Z., Saliganan A., Che M., Bonfil D., Cher M., Sarkar F.H.
Cancer Research, 2007
3.
In VitroInhibitory and Cytotoxic Activity of MFM 501, a Novel Codonopsinine Derivative, against Methicillin-ResistantStaphylococcus aureusClinical Isolates
Johari S.A., Mohtar M., Syed Mohammad S.A., Sahdan R., Shaameri Z., Hamzah A.S., Mohammat M.F.
BioMed Research International, 2015
5.
Sukhanova A.A., Nelyubina Y.V., Zlotin S.G.
Mendeleev Communications, 2016
7.
Khasiyatullina N.R., Vazykhova A.M., Mironov V.F., Krivolapov D.B., Voronina Y.K., Voloshina A.D., Kulik N.V., Strobykina A.S.
Mendeleev Communications, 2017
8.
Synthesis of 2-(2-hydroxyaryl)alkenylphosphonium salts from phosphine oxides via ring-closing ring-opening approach and their antimicrobial evaluation
Tatarinov D.A., Kuznetsov D.M., Voloshina A.D., Lyubina A.P., Strobykina A.S., Mukhitova F.K., Polyancev F.M., Mironov V.F.
Tetrahedron, 2016
9.
D. Haebich, J. Hansen and A. Paessens, EP0472077, 1992.
10.
Structural diversity of nucleoside phosphonic acids as a key factor in the discovery of potent inhibitors of rat T-cell lymphoma thymidine phosphorylase
Kočalka P., Rejman D., Vaněk V., Rinnová M., Tomečková I., Králíková Š., Petrová M., Páv O., Pohl R., Buděšínský M., Liboska R., Točík Z., Panova N., Votruba I., Rosenberg I., et. al.
Bioorganic and Medicinal Chemistry Letters, 2010
11.
N-Phosphonocarbonylpyrrolidine Derivatives of Guanine: A New Class of Bi-Substrate Inhibitors of Human Purine Nucleoside Phosphorylase
Rejman D., Panova N., Klener P., Maswabi B., Pohl R., Rosenberg I.
Journal of Medicinal Chemistry, 2012
12.
Inhibition of the Escherichia coli 6-Oxopurine Phosphoribosyltransferases by Nucleoside Phosphonates: Potential for New Antibacterial Agents
Keough D.T., Hocková D., Rejman D., Špaček P., Vrbková S., Krečmerová M., Eng W.S., Jans H., West N.P., Naesens L.M., de Jersey J., Guddat L.W.
Journal of Medicinal Chemistry, 2013
13.
New Phosphorylated Derivatives of Piperidine and Pyrrolidine
Şener Ş., Mete A.
Synthetic Communications, 1997
14.
A practical method of preparing optically active dialkyl phenyl phosphates
Koizumi T., Kobayashi Y., Amitani H., Yoshii E.
Journal of Organic Chemistry, 1977
15.
Synthesis and novel properties of N-phosphoryl peptides
Ma X., Zhao Y.
Journal of Organic Chemistry, 1989
16.
A highly enantioselective synthesis of phosphate triesters
Nakayama K., Thompson W.J.
Journal of the American Chemical Society, 1990
17.
10.1016/j.mencom.2018.07.019_sbref0065a
Kowalczyk
Synthesis, 2017
18.
10.1016/j.mencom.2018.07.019_sbref0065b
Subotkowski
Pol. J. Chem, 1980
19.
Pyrrolidine N-alkylphosphonates and related nucleotide analogues: synthesis and stereochemistry
Rejman D., Pohl R., Kočalka P., Masojídková M., Rosenberg I.
Tetrahedron, 2009
20.
A new synthetic method for proline diphenyl phosphonates
Belyaev A., Borloo M., Augustyns K., Lambeir A., De Meester I., Scharpe S., Blaton N., Peeters O.M., De Ranter C., Haemers A.
Tetrahedron Letters, 1995
21.
Structure−Activity Relationship of Diaryl Phosphonate Esters as Potent Irreversible Dipeptidyl Peptidase IV Inhibitors
Belyaev A., Zhang X., Augustyns K., Lambeir A., De Meester I., Vedernikova I., Scharpé S., Haemers A.
Journal of Medicinal Chemistry, 1999
22.
5-Diethoxyphosphoryl-5-methyl-1-pyrroline N-oxide (DEPMPO): a new phosphorylated nitrone for the efficient In Vitro and In Vivo spin trapping of oxygen-centred radicals
Frejaville C., Karoui H., Tuccio B., le Moigne F., Culcasi M., Pietri S., Lauricella R., Tordo P.
Journal of the Chemical Society Chemical Communications, 1994
23.
Synthesis and antibacterial evaluation of phosphonic acid analogues of diaminopimelic acid
van Assche I., Soroka M., Haemers A., Hooper M., Blanot D., van Heijenoort J.
European Journal of Medicinal Chemistry, 1991
25.
Anti-human immunodeficiency activity of novel 2-arylpyrrolidine analogs
Martirosyan A.H., Gasparyan S.P., Alexanyan M.V., Harutyunyan G.K., Panosyan H.A., Schinazi R.F.
Medicinal Chemistry Research, 2016
26.
Matyugina E.S., Valuev-Elliston V.T., Chizhov A.O., Kochetkov S.N., Khandazhinskaya A.L.
Mendeleev Communications, 2016
27.
Gaman M.S., Matyugina E.S., Novikov M.S., Babkov D.A., Solyev P.N., Kochetkov S.N., Khandazhinskaya A.L.
Mendeleev Communications, 2017
28.
Synthesis of novel 2-arylpyrrolidines by the reaction of 1-(4,4-diethoxybutyl)urea with resorcinols
Smolobochkin A.V., Gazizov A.S., Vagapova L.I., Burilov A.R., Pudovik M.A.
Russian Chemical Bulletin, 2014
29.
Facile synthesis of 2-(2-arylpyrrolidin-1-yl)pyrimidines via acid-catalyzed reaction of N-(4,4-diethoxybutyl)pyrimidin-2-amine with phenols
Gazizov A.S., Kharitonova N.I., Smolobochkin A.V., Syakaev V.V., Burilov A.R., Pudovik M.A.
Monatshefte fur Chemie, 2015
30.
β- and γ-amino acetals containing phosphine oxide groups. Synthesis and reactions with resorcinol derivatives
Vagapova L.I., Amirova L.R., Burilov A.R., Garifzyanov A.R., Pudovik M.A., Kharlampidi K.E.
Russian Journal of Organic Chemistry, 2014