Search Results - "Kawakubo, Masato"
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Synthesis, Structural Characterization, and Optical Properties of Benzene-Fused Tetracyclic and Pentacyclic Stiboles
Published in Molecules (Basel, Switzerland) (04-01-2021)“…The expectation that antimony (Sb) compounds should display phosphorescence emissions based on the "heavy element effect" prompted our interest in the…”
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Synthesis, structural characterization, and optical properties of benzo[ f ]naphtho[2,3- b ]phosphoindoles
Published in Beilstein journal of organic chemistry (05-03-2021)“…Phosphole-fused π-conjugated acenes have been attracting interest because of the attractive features of the phosphole moiety, such as fluorescence and…”
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Synthesis of novel 5-iodopyrido[1′,2′;2,3]imidazo[5,1-a]isoquinolinium iodides from 2-(2-ethynylphenyl)imidazo[1,2-a]pyridines via iodocyclization
Published in Tetrahedron letters (31-08-2022)“…[Display omitted] The iodocyclization of alkynes is a facile method for synthesizing essential heterocycles. A simple synthesis for novel 5-iodo-6-substituted…”
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Novel mono substituted pyridoimidazoisoquinoliniums via a silver-catalyzed intramolecular cyclization and their applications in cellular imaging
Published in RSC advances (20-03-2024)“…Cationic heterocycles, an important class of organic compounds soluble in polar solvents, have been gaining attention in the construction of fluorescent…”
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Synthesis and Optical Properties of Azuleno[1,2-b]benzothiophene and Selenophene
Published in Heterocycles (2022)Get full text
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Novel mono substituted pyridoimidazoisoquinoliniums a silver-catalyzed intramolecular cyclization and their applications in cellular imaging
Published in RSC advances (22-03-2024)“…Cationic heterocycles, an important class of organic compounds soluble in polar solvents, have been gaining attention in the construction of fluorescent…”
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Synthesis and Intracellular Localization of 5,6‐Disubsutituted Pyrido[1′,2′;2,3]imidazo[5,1‐a]isoquinolinium Iodides
Published in ChemistrySelect (Weinheim) (20-11-2023)“…Novel pyrido[1’,2’;2,3]imidazo[5,1‐a]isoquinolinium iodides independently substituted at their 5‐ and 6‐position were prepared from…”
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