V. G. Mairanovskii

Russian Academy of Sciences

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ТМ

Т. М. Филиппова

Angarsk State Technical Academy

N. T. Ioffe

Institute of Problems of Chemical Physics

L. Yu. Yuzefovich

G. I. SAMOKHVALOV

Research Institute of Scientific Research and Production Association

B. M. Sheiman

I. A. Titova

A.E. Favorsky Irkutsk Institute of Chemistry

ВВ

В. В. Мищенко

Odessa National Medical University

N. F. LOGINOVA

N. A. Bogoslovskii

National Academy of Sciences of Ukraine

A. A. Engovatov

NovaBiotics (United Kingdom)

Cooperative Institutions

Russian Academy of Sciences

NovaBiotics (United Kingdom)

Moscow Technological Institute

Lomonosov Moscow State University

Research Institute of Scientific Research and Production Association

Latvian Academy of Sciences

N.D. Zelinsky Institute of Organic Chemistry

Moscow State University of Fine Chemical Technologies

Semenov Institute of Chemical Physics

Moscow Architectural Institute

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ChemInform Abstract: DIE ABSPALTUNG EINER TOSYLSCHUTZGRUPPE MITTELS ELEKTROCHEMISCHER RED. IN DIMETHYLFORMAMID

Chemischer Informationsdienst (1972)

V. G. Mairanovskii N. F. LOGINOVA

Abstract Es ist bekannt, Tosylschutzgruppen durch elektrochemische Reduktion in einer 1 m methanolischen Lösung von Tetramethylammoniumchlorid abzuspalten.

10.1002/chin.197214200

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Structure of the side product in the preparation of 4-methyl-5-(β-hydroxyethyl)thiazole

Pharmaceutical Chemistry Journal (1982)

Т. М. Филиппова A. R. Bekker T. I. Ozorova V. M. Belova V. G. Mairanovskii

Thiazole

10.1007/bf00762036

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Kinetics of symmetric electron exchange reaction in series of substituted nitrobenzenes: Influence of reactant structure

Theoretical and Experimental Chemistry (1989)

N. T. Ioffe V. G. Mairanovskii

Nitrobenzene

10.1007/bf00534443

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ChemInform Abstract: ELEKTROCHEMISCHE ABSPALTUNG VON SCHUTZGRUPPEN, ANWENDUNG AKTIVIERENDER SUBSTITUENTEN

Chemischer Informationsdienst (1973)

V. G. Mairanovskii N. F. LOGINOVA

Abstract Die elektrochemische Abspaltung von Schutzgruppen ist bekannt, erfordert aber Kathodenpotentiale von ‐E 2,0 ‐ 2,8 V. Dadurch ist die Anwendung dieser Methode auf solche Stoffe beschränkt, die keine anderen elektrochemisch aktiven Gruppen enthalten.

10.1002/chin.197319109

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Citations (1)

Spectrophotometric analysis of the products of oxidative ammonolysis in the production of nicotinic acid

Pharmaceutical Chemistry Journal (1976)

В. В. Мищенко A. K. Starostina I. I. Stroganova Э. М. Гусейнов V. G. Mairanovskii

10.1007/bf00758113

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Mechanism of the ring-chain tautomerism of 2,3,3-trimethyl-2-hydroxy-5-pyrrolidones

Chemistry of Heterocyclic Compounds (1979)

L. Yu. Yuzefovich B. M. Sheiman V. G. Mairanovskii Т. М. Филиппова

Chain (unit)

10.1007/bf00773214

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Prediction of the catalytic activity of cobalt pyridines in the reaction involving chain transfer to the monomer using polarographic half-wave potentials

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science (1988)

B.R. Smirnov V. G. Mairanovskii I. M. Muratov N. S. Enikolopyan

Polarography

Chain (unit)

Chain transfer

Chain reaction

10.1007/bf00961956

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Spectrophotometric analysis of multicomponent mixtures of 3,5-dinitrobsnzoates in the production of vitamin D2

Pharmaceutical Chemistry Journal (1976)

В. В. Мищенко G. K. Shostakovskaya N. A. Bogoslovskii A. N. Gusarov V. G. Mairanovskii

10.1007/bf00758059

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ChemInform Abstract: ELECTROCHEMICAL SYNTHESIS OF MESOMETHYLPORPHYRINS FROM ALKOXYMETHYLPORPHYRINS

Chemischer Informationsdienst (1980)

V. G. Mairanovskii N. T. Ioffe R. Marinova Г.В. Пономарев

Abstract Die Meso‐alkoxymethylphorphyrine (Ia) und (Ib) lassen sich elektrochemisch quantitativ zur Mesomethylverbindung (Ic) reduzieren.

10.1002/chin.198030325

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ChemInform Abstract: ELEKTROCHEMISCHE ABSPALTUNG VON BENZYLIDEN‐ UND BENZOYL‐SCHUTZGRUPPEN BEI KOHLENHYDRATEN

Chemischer Informationsdienst (1974)

V. G. Mairanovskii N. F. LOGINOVA A. M. Ponomarev A. YA. VEINBERG

Abstract Die Schutzgruppen von β‐D‐Methyl‐2‐benzoyl‐4,6‐benzylidengalaktopyranosid lassen sich durch Elektrolyse an einer Hg‐Kathode in Dimethylformamid (1% Tetrabutylam‐ moniumjodid enthaltend) bei 25°C glatt entfernen.

10.1002/chin.197414143

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