Olga Mikhailovna Mulina

Olga Mikhailovna Mulina

Auto-generated profile, based on publicly available information

Olga Mikhailovna Mulina

Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prospect, Moscow, 119991, Russian Federation

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
2 August 2020 in Advanced Synthesis & Catalysis
Verified
Journal Article
Closed access
PDF file
OMOlga M. Mulina
Olga M. Mulina
AIAlexey I. Ilovaisky
Alexey I. Ilovaisky
VPVadim D. Parshin
Vadim D. Parshin
Alexander Terent'evAlexander Terent'ev
Alexander Terent'ev

23 August 2018 in European Journal of Organic Chemistry
Verified
Journal Article
Closed access
PDF file
OMOlga M. Mulina
Olga M. Mulina
AIAlexey I. Ilovaisky
Alexey I. Ilovaisky
Alexander Terent'evAlexander Terent'ev
Alexander Terent'ev

20 February 2020 in Organic Letters
Verified
Journal Article
Closed access
OMOlga M. Mulina
Olga M. Mulina
NZNataliya V. Zhironkina
Nataliya V. Zhironkina
SPStanislav A. Paveliev
Stanislav A. Paveliev
DDDmitry V. Demchuk
Dmitry V. Demchuk
Alexander Terent'evAlexander Terent'ev
Alexander Terent'ev

11 March 2020 in Organic Letters
Verified
Journal Article
Closed access
LKLisa Marie Kammer
Lisa Marie Kammer
MKMatthias Krumb
Matthias Krumb
BSBenjamin Spitzbarth
Benjamin Spitzbarth
BLBenjamin Lipp
Benjamin Lipp
JKJonas Kühlborn
Jonas Kühlborn
TOTill Opatz
Till Opatz

1 December 2017 in Tetrahedron
Verified
Journal Article
Closed access
Alexander Terent'evAlexander Terent'ev
Alexander Terent'ev
OMOlga M. Mulina
Olga M. Mulina
DPDmitry A. Pirgach
Dmitry A. Pirgach
AIAlexey I. Ilovaisky
Alexey I. Ilovaisky
MSMikhail Syroeshkin
Mikhail Syroeshkin
GNGennady I. Nikishin
Gennady I. Nikishin

14 September 2016 in RSC Advances
Verified
Journal Article
Open access
PDF file
Alexander Terent'evAlexander Terent'ev
Alexander Terent'ev
OMOlga M. Mulina
Olga M. Mulina
DPDmitry A. Pirgach
Dmitry A. Pirgach
DDDmitry V. Demchuk
Dmitry V. Demchuk
MSMikhail Syroeshkin
Mikhail Syroeshkin
GNGennady I. Nikishin
Gennady I. Nikishin
Copper(I) halides were used as mediators in the synthesis of β-hydroxysulfones via the oxysulfonylation of styrenes using sulfonylhydrazides. The feature of the developed process lies in the combination of a copper(I) salt with oxygen—the stoichiometric oxidant. Copper(II) species are responsible for the oxidation of sulfonylhydrazides, they are generated in small amounts in the O2/Cu(I)/Cu(II) redox system, which is formed during the reaction. The combination of these three components enables one to obtain in the case of α-methylstyrenes only β-hydroxysulfones and in the case of α-unsubstituted styrenes, β-hydroxysulfones as the main products and β-ketosulfones as the by-products. With good yields β-hydroxysulfones were prepared by reduction of the reaction mixture containing both products β-hydroxysulfones and β-ketosulfones with NaBH4. An electrochemical study revealed that the Cu(I)/Cu(II) pair can serve as an effective mediator of β-hydroxysulfones formation via redox processes.