Search Results - "Stepakov, Alexander V"
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Identification of Spiro-Fused Pyrrolo[3,4- a ]pyrrolizines and Tryptanthrines as Potential Antitumor Agents: Synthesis and In Vitro Evaluation
Published in International journal of molecular sciences (05-11-2021)“…A series of heterocyclic compounds containing a spiro-fused pyrrolo[3,4- ]pyrrolizine and tryptanthrin framework have been synthesized and studied as potential…”
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Identification of Spiro-Fused [3-azabicyclo[3.1.0]hexane]oxindoles as Potential Antitumor Agents: Initial In Vitro Evaluation of Anti-Proliferative Effect and Actin Cytoskeleton Transformation in 3T3 and 3T3-SV40 Fibroblast
Published in International journal of molecular sciences (31-07-2021)“…Novel heterocyclic compounds containing 3-spiro[3-azabicyclo[3.1.0]hexane]oxindole framework ( , and ) have been studied as potential antitumor agents. The in…”
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11H-Benzo[4,5]imidazo[1,2-a]indol-11-one as a New Precursor of Azomethine Ylides: 1,3-Dipolar Cycloaddition Reactions with Cyclopropenes and Maleimides
Published in International journal of molecular sciences (01-11-2022)“…The possibility of generating azomethine ylides from 11H-benzo[4,5]imidazo[1,2-a]indol-11-one and amino acids is shown for the first time. Based on the…”
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Biological Evaluation of 3-Azaspiro[Bicyclo[3.1.0]Hexane-2,5′-Pyrimidines] as Potential Antitumor Agents
Published in International journal of molecular sciences (15-09-2022)“…A series of heterocyclic compounds containing spirofused barbiturate and 3-azabicyclo[3.1.0]hexane frameworks have been studied as potential antitumor agents…”
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Synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexane via cyclopropene cycloadditions to the stable azomethine ylide derived from Ruhemann's purple
Published in Beilstein journal of organic chemistry (29-06-2022)“…A reliable method for the synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexanes through the 1,3-dipolar cycloaddition (1,3-DC) reactions of…”
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Stereo- and Regioselective 1,3-Dipolar Cycloaddition of the Stable Ninhydrin-Derived Azomethine Ylide to Cyclopropenes: Trapping of Unstable Cyclopropene Dipolarophiles
Published in Journal of organic chemistry (07-06-2019)“…A stereo- and regioselective 1,3-dipolar cycloaddition of the stable ninhydrin-derived azomethine ylide…”
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Synthesis of Functionalized 3‑Spiro[cyclopropa[a]pyrrolizine]- and 3‑Spiro[3-azabicyclo[3.1.0]hexane]oxindoles from Cyclopropenes and Azomethine Ylides via [3 + 2]-Cycloaddition
Published in Journal of organic chemistry (20-01-2017)“…3-Spiro[cyclopropa[a]pyrrolizine]- and 3-spiro[3-azabicyclo[3.1.0]hexane]oxindoles were prepared in moderate to high yields via one-pot three-component…”
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Diastereomers of Cyclopropa[a]pyrrolizine Spiro-fused with a Benzo[4,5]imidazo[1,2-a]indole Fragment: Structure Determinations Using NMR Methods
Published in Applied magnetic resonance (01-10-2023)“…NMR spectroscopy methods have been used to prove structures of two diastereomers of cyclopropa[ a ]pyrrolizine spiro-fused with a benzo[4,5]imidazo[1,2- a…”
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NMR Study of Spatial Structure and Internal Dynamic of Adducts of Ninhydrin-Derived Azomethine Ylide with Cyclopropenes
Published in Applied magnetic resonance (01-02-2020)“…Using NMR spectroscopy, the structure of the new products obtained in reaction of ninhydrin-derived azomethine ylide with cyclopropenes was established and…”
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Regioisomers of 2,5,6,7,8-Pentaaryl-1H-Azepino[3,2,1-ij]Quinazoline-1,3(2H)-Dione Containing Various Aryl Substituents in the Azepine Ring: Structure Determination Using NMR Methods
Published in Applied magnetic resonance (01-12-2022)“…NMR spectroscopy methods were used to prove the structures of two similar regioisomers of 2,5,6,7,8-pentaaryl-1 H -azepino[3,2,1- ij ]quinazoline-1,3(2 H…”
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A highly efficient [3+2] cycloaddition of nitrile oxides and azomethine imines to N-vinylpyrroles
Published in Tetrahedron (08-04-2015)“…1,3-Dipolar cycloaddition of various nitrile oxides to substituted N-vinylpyrroles proceed with high efficiency and selectivity with the formation of single…”
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[3+2] Cycloaddition reactions of arylallenes with C-(N-arylcarbamoyl)- and C,C-bis(methoxycarbonyl)nitrones and subsequent rearrangements
Published in Tetrahedron letters (02-07-2014)“…The first example of 1,3-dipolar cycloaddition reactions of nitrones with arylallenes is described. C-Carbamoylnitrones react with the C1C2 double bond of…”
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Synthesis of indene derivatives via reactions of vinylidenecyclopropanes with the N-acyliminium cations generated from hydroxylactams
Published in Tetrahedron letters (19-03-2014)“…A novel route for the synthesis of 1H-indene derivatives via the reactions of vinylidenecyclopropanes (VCPs) with the N-acyliminium cations generated from…”
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Acid-induced rearrangement of cycloadducts from N-aryl itaconimides and 1,3-diphenylisobenzofuran
Published in Tetrahedron letters (27-08-2014)“…Treatment of several Diels–Alder adducts of N-aryl itaconimides and 1,3-diphenylisobenzofuran with a strong acid triggers a skeletal rearrangement resulting in…”
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Acid-Induced Rearrangement of Cycloadducts from Cyclopropenecarboxylates and 1,3-Diarylisobenzofurans
Published in Helvetica chimica acta (01-07-2016)“…Treatment of several Diels–Alder adducts of cyclopropenecarboxylates and 1,3‐diarylisobenzofurans with a strong acid triggers a skeletal rearrangement…”
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Reactions of 1,1-diaryl-2-isopropylidene-3-methylenecyclopropanes with C,N-diarylnitrones and nitrile oxides
Published in Tetrahedron letters (04-07-2012)“…The reactions of unactivated bis(methylene)cyclopropanes with nitrones and nitrile oxides have been investigated. The…”
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The first example of 1,3-dipolar cycloaddition reactions of nitrones to vinylidenecyclopropanes
Published in Tetrahedron letters (02-11-2011)“…The first example of 1,3-dipolar cycloaddition reactions of nitrones to vinylidenecyclopropanes is described. The nitrones react with the C1′–C2′ double bond…”
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A new approach to the synthesis of 4-( N-aryl)carbamoylmethyl-4,5-dihydropyridazin-3(2 H)-ones
Published in Tetrahedron letters (15-06-2011)“…Reaction of N-aryl substituted maleimides with aliphatic ketazines leads to the formation of 4,5-dihydropyridazin-3(2 H)-ones in moderate yields. The reaction…”
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Diastereoselective 1,3-dipolar cycloaddition of cyclopropenes to acenaphthenequinone azomethine ylides
Published in Tetrahedron (30-01-2024)Get full text
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