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N. A. Bogoslovskii

National Academy of Sciences of Ukraine

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G. I. SAMOKHVALOV

Research Institute of Scientific Research and Production Association

G. E. Litvinova

Latvian Academy of Sciences

V. K. Bauman

Institute of Bioorganic Chemistry and Petrochemistry V.P. Kukhar

M. Yu. Valinietse

Latvian State Forest Research Institute "Silava"

Т. М. Филиппова

Angarsk State Technical Academy

T. A. Kisel'nikova

Latvian Academy of Sciences

Dmitry Babarykin

State Forest Research Institute

V. G. Mairanovskii

Russian Academy of Sciences

V. B. Spirichev

Institute of Pharmacology Russian Academy of Medical Sciences

I. P. Terenetskaya

Institute of Physics

Cooperative Institutions

Russian Academy of Sciences

Lomonosov Moscow State University

All-Russian State Scientific Research Institute for Control, Standardization and Certification of Veterinary Preparations

Latvian Academy of Sciences

Moscow State University of Fine Chemical Technologies

N.D. Zelinsky Institute of Organic Chemistry

Institute of Physics

Concern Energomera (Russia)

Farmak (Czechia)

NovaBiotics (United Kingdom)

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Spectrophotometric determination of 1α-hydroxycholecalciferol

Pharmaceutical Chemistry Journal (1980)

I. P. Pushkina É. A. Petrova N. A. Bogoslovskii N. A. Ulanova L. V. Prokhorova

10.1007/bf00765670

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Synthesis and biological activity of 22-dehydrovitamin D3 and 22-dehydro-25-hydroxyvitamin D3

Pharmaceutical Chemistry Journal (1978)

G. E. Litvinova N. A. Bogoslovskii V. K. Bauman M. Yu. Valinietse Dmitry Babarykin

10.1007/bf00777947

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Activity of 5,6-trans- and 22-dehydro-analogs of 1,25-dihydroxyvitamin D3

Pharmaceutical Chemistry Journal (1984)

I. A. Alekseeva V. B. Spirichev N. V. Blazheevich S. V. Sokolova N. A. Bogoslovskii

10.1007/bf00776787

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A study of the products of the autooxidation of vitamin D I. Nonpolar products of the oxidative degradation of vitamin D2

Chemistry of Natural Compounds (1971)

Z. P. Kozhina N. A. Bogoslovskii V. B. Spirichev Е. В. Кабанова

Autoxidation

Aqueous medium

Peroxide

Degradation

10.1007/bf00564738

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Synthesis and biological activity of 1α-hydroxyvitamin D3 1-butyrate

Pharmaceutical Chemistry Journal (1987)

N. A. Bogoslovskii V. K. Bauman M. Yu. Valinietse Dmitry Babarykin T. A. Kisel'nikova

10.1007/bf00758760

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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: DIE SYNTHESE VON VITAMIN D3 AUS ERGOSTERIN

Chemischer Informationsdienst (1974)

N. A. Bogoslovskii Sh. S. Levi R. P. EVSTIGNEEVA N. P. Lazareva É. A. Petrova

Abstract Aus dem Ergosterin (I) wird über das Peroxid (II) durch Veränderung der Seitenkette mit Hilfe einer Ozonspaltung und einer Wittigsynthese nach der Neubildung des Dien‐Systems die Vorstufe (X) des Vitamins D3 hergestellt, aus der durch Belichtung das Vitamin B3 entsteht.

10.1002/chin.197439473

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Citations (1)

Comparative biological activity of 1,25-dihydroxy-vitamin D3 and its 5,6-trans-isomer

Pharmaceutical Chemistry Journal (1986)

M. Yu. Valinietse V. K. Bauman Dmitry Babarykin N. A. Bogoslovskii T. A. Kisel'nikova

10.1007/bf00758556

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Relative biological activity of vitamins D2, D3 and their 1α-hydroxy analogs in the chicken

Pharmaceutical Chemistry Journal (1982)

V. K. Bauman M. Yu. Valinietse Dmitry Babarykin N. A. Bogoslovskii

10.1007/bf00770319

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Routes to optimization of previtamin D photosynthesis using irradiation by a sunlamp

Pharmaceutical Chemistry Journal (1994)

I. P. Terenetskaya N. A. Bogoslovskii L. N. Vysotskii F. I. Luknitskii

10.1007/bf02219037

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Citations (6)