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Molecules (Basel, Switzerland)|September 28, 2021
Terpene Research Is Providing New Inspiration for ScientistsPavel B Drasar, Vladimir A KhripachMolecules (Basel, Switzerland)|December 22, 2019
Growing Importance of Natural Products ResearchPavel B Drasar, Vladimir A KhripachMolecules (Basel, Switzerland)|April 12, 2022
Structure and Biological Activity of Ergostane-Type Steroids from FungiVladimir N Zhabinskii, Pavel Drasar, Vladimir A KhripachSteroids|April 16, 2013
1,4-Chirality transfer via the ester enolate Claisen rearrangements in the preparation of (25R)- and (25S)-cholestenoic acidsYurii V Ermolovich, Vladimir N Zhabinskii, Vladimir A KhripachThe Journal of Steroid Biochemistry and Molecular Biology|February 19, 2013
Synthesis of fatty acyl derivatives of 24-epibrassinolideVladimir A Khripach, Vladimir N Zhabinskii, Dmitrii V TsavlovskiiSteroids|September 15, 2014
Steroid plant hormones: effects outside plant kingdomVladimir N Zhabinskii, Natalia B Khripach, Vladimir A KhripachSteroids|April 11, 2012
A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: application to the preparation of early brassinolide biosynthetic precursorsAlaksiej L Hurski, Vladimir N Zhabinskii, Vladimir A KhripachSteroids|October 7, 2004
Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl esterAndrey P Antonchick, Bernd Schneider, Vladimir N Zhabinskii, et al.Steroids|December 25, 2012
Diels-Alder reaction of androsta-14,16-dien-17-yl acetates with nitroethylene: product distribution and selected adduct transformationsAlexander V Baranovsky, Dmitry A Bolibrukh, Vladimir A Khripach, et al.Steroids|September 8, 2014
A new synthesis of brassinosteroids with a cholestane framework based on a highly functionalized starting materialIrina D Alshakova, Yuri V Ermolovich, Vladimir N Zhabinskii, et al.Pageof 6