Sergey V. Dubovitskii

The first syntheses of 3-bromofascaplysin, 10-bromofascaplysin and 3,10-dibromofascaplysin—marine alkaloids from Fascaplysinopsis reticulata and Didemnum sp. by application of a simple and effective approach to the pyrido[1,2-a:3,4-b′]diindole system

Maxim E. Zhidkov, Olga V. Baranova, N. N. Balaneva et al. · Tetrahedron Letters · 2007 · 39 citations

Diversity Oriented Synthesis, Bioorganic Chemistry, Biochemistry +11

A new method for the synthesis of the marine alkaloid fascaplysin

Maxim E. Zhidkov, Olga V. Baranova, Natalya S. Kravchenko et al. · Tetrahedron Letters · 2010 · 32 citations

Biosynthesis, Bioorganic Chemistry, Biochemistry +7

Method for synthesis of 12H-pyrido[1,2-a:3,4-b']diindoles. Total synthesis of homofascaplysin C

Sergey V. Dubovitskii · Tetrahedron Letters · 1996 · 25 citations

Natural Sciences, Diversity-oriented Synthesis, Total Synthesis +5

Synthesis of isocryptolepine, an alkaloid fromCryptolepis sanguinolenta

Sergey V. Dubovitskii, Oleg S. Radchenko, V. L. Norikov · Russian Chemical Bulletin · 1996 · 13 citations

Alkaloid Fromcryptolepis Sanguinolenta, Phytochemistry, Pharmacology +2

An unexpected rearrangement of 3-unsubstituted-2-acyl substituted indole phenylhydrazones. A new method for benz[c]β-carboline synthesis

Olga V. Baranova, Sergey V. Dubovitskii · Tetrahedron Letters · 2003 · 10 citations

Diversity Oriented Synthesis, Natural Sciences, Diversity-oriented Synthesis +6