Home / Publications / Selenazolium salts as catalysts in oxidation reactions

Selenazolium salts as catalysts in oxidation reactions

Pavel Arsenyan 1
Pavel Arsenyan
, 
Jelena Vasiljeva 1
Jelena Vasiljeva
10.1016/j.mencom.2017.11.028
Published 2017-10-30
Communication , Volume 27, Issue 6, 621-622
7
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Arsenyan P., Vasiljeva J. Selenazolium salts as catalysts in oxidation reactions // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 621-622.
GOST all authors (up to 50) Copy
Arsenyan P., Vasiljeva J. Selenazolium salts as catalysts in oxidation reactions // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 621-622.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2017.11.028
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.028
TI - Selenazolium salts as catalysts in oxidation reactions
T2 - Mendeleev Communications
AU - Arsenyan, Pavel
AU - Vasiljeva, Jelena
PY - 2017
DA - 2017/10/30
PB - Mendeleev Communications
SP - 621-622
IS - 6
VL - 27
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2017_Arsenyan,
author = {Pavel Arsenyan and Jelena Vasiljeva},
title = {Selenazolium salts as catalysts in oxidation reactions},
journal = {Mendeleev Communications},
year = {2017},
volume = {27},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.028},
number = {6},
pages = {621--622},
doi = {10.1016/j.mencom.2017.11.028}
}
MLA
Cite this
MLA Copy
Arsenyan, Pavel, and Jelena Vasiljeva. “Selenazolium salts as catalysts in oxidation reactions.” Mendeleev Communications, vol. 27, no. 6, Oct. 2017, pp. 621-622. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.028.

Abstract

Selenazolium salts promote mild oxidation of 2-aminophenol, hydroquinone, Trolox-C, and anthracene with hydrogen peroxide.

References

1.
Selenocysteine in proteins—properties and biotechnological use
Johansson L., Gafvelin G., Arnér E.S.
Biochimica et Biophysica Acta - General Subjects, 2005
2.
10.1016/j.mencom.2017.11.028_bib0010
Flohé
Its Molecular Biology and Role in Human Health, 2012
4.
10.1016/j.mencom.2017.11.028_bib0020
Socha
Nutr. J., 2014
5.
10.1016/j.mencom.2017.11.028_bib0025
Batist
Cancer Res., 1986
6.
Fused Selenazolinium Salt Derivatives with a Se-N+Bond: Preparation and Properties
Arsenyan P., Vasiljeva J., Belyakov S., Liepinsh E., Petrova M.
European Journal of Organic Chemistry, 2015
7.
Selenium analogues of ( S )-clopidogrel: preparation method and properties
Vasiljeva J., Domracheva I., Arsenyan P.
Tetrahedron Letters, 2016
9.
Arsenyan P., Vasiljeva J., Belyakov S., Petrova M., Liepinsh E.
Mendeleev Communications, 2016
10.
Phenoxazinone synthase: what's in a name?
Le Roes-Hill M., Goodwin C., Burton S.
Trends in Biotechnology, 2009
11.
Laccase-mediated formation of the phenoxazinone derivative, cinnabarinic acid
Eggert C., Temp U., Dean J.F., Eriksson K.L.
FEBS Letters, 1995
13.
Antitumor Agents. 1. Synthesis, Biological Evaluation, and Molecular Modeling of 5H-Pyrido[3,2-a]phenoxazin-5-one, a Compound with Potent Antiproliferative Activity
Bolognese A., Correale G., Manfra M., Lavecchia A., Mazzoni O., Novellino E., Barone V., Pani A., Tramontano E., La Colla P., Murgioni C., Serra I., Setzu G., Loddo R.
Journal of Medicinal Chemistry, 2002
14.
Iwata A., Yamaguchi T., Sato K., Izumi R., Tomoda A.
Tohoku Journal of Experimental Medicine, 2003
15.
10.1016/j.mencom.2017.11.028_bib0075
Schimamoto
Clin. Cancer Res., 2001
16.
Catalytic Oxidative Cyclocondensation ofo‐Aminophenols to 2‐Amino‐3H‐phenoxazin‐3‐ones
Giurg M., Piekielska K., Gębala M., Ditkowski B., Wolański M., Peczyńska‐Czoch W., Młochowski J.
Synthetic Communications, 2007
17.
Copper(II) nanoparticles: an efficient and reusable catalyst in green oxidation of benzyl alcohols to benzaldehydes in water
Mirsafaei R., Heravi M.M., Hosseinnejad T., Ahmadi S.
Applied Organometallic Chemistry, 2016
19.
10.1016/j.mencom.2017.11.028_bib0095
Engin
Mol. Vis., 2009
22.
Simple and economical conversion of organic compounds with H2O2 catalyzed by ruthenium (III) chloride
Tandon P.K., Baboo R., Singh A.K., Gayatri
Applied Organometallic Chemistry, 2005
23.
Młochowski J., Brząszcz M., Chojnacka M., Giurg M., Wójtowicz H.
Arkivoc, 2004