Larisa N. Kulikova
Peoples' Friendship University of Russia
70 Papers
245 Citations
Larisa N. Kulikova is an academic researcher from Peoples' Friendship University of Russia. The author has contributed to research in topics: Ring (chemistry) & Ethyl propiolate. The author has an hindex of 11, co-authored 65 publications.
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Papers
Tetrahydropyridine (THP) ring expansion under the action of activated terminal alkynes. The first synthesis and X-ray crystal structure of tetrahydropyrimido[4,5- d ]azocines
Leonid G. Voskressensky,Tatiana N. Borisova,Innokenti S. Kostenev,Larisa N. Kulikova,Alexey V. Varlamov +4 more
TL;DR: Tetrahydropyridopyrimidines (THPPm) as discussed by the authors are representative of a new heterocyclic system and undergo tandem cleavage-cyclization piperidine ring enlargement under the action of terminal activated alkynes.
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Tandem enlargement of the tetrahydropyridine ring in 1-aryl-tetrahydroisoquinolines using activated alkynes—a new and effective synthesis of benzoazocines
Leonid G. Voskressensky,Tatiana N. Borisova,Anna V. Listratova,Larisa N. Kulikova,Alexander A. Titov,Alexey V. Varlamov +5 more
TL;DR: Tetrahydroisoquinolines 3a-e underwent piperidine ring enlargement under the action of activated alkynes, giving benzoazocines 4, 5 and 7-11 in high yields as mentioned in this paper.
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Investigation on the antiplatelet activity of pyrrolo[3,2-c]pyridine-containing compounds.
Leonid G. Voskressensky,Modesto de Candia,Andrea Carotti,Tatiana N. Borisova,Larisa N. Kulikova,Alexey V. Varlamov,Cosimo Altomare +6 more
TL;DR: A relation between activity and calculated octanol‐water partition coefficient suggested that a log P value around 2.5 should be the optimal lipophilicity value for the activity of THPP‐containing compounds.
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Cleavage of some annulated tetrahydropyridines under the action of dimethyl acetylene dicarboxylate in protic solvents. New practical route to substituted pyrroles and indoles.
Tatiana N. Borisova,Leonid G. Voskressensky,Tatiana A. Soklakova,Larisa N. Kulikova,Alexey V. Varlamov +4 more
TL;DR: Tetrahydropyrrolo[3,2-c]pyridines and tetrahYDropyrido[4,3-b]indoles undergo piperidine ring opening under the action of dimethyl acetylene dicarboxylate in alcohols or in aqueous dioxane, providing β-substituted pyrroles (indoles) in moderate to high yields.
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