Academic literature on the topic 'Isochromen-1-one'

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Journal articles on the topic "Isochromen-1-one"

1

Hlotov, Serhii, Olga Shablykina, and Volodymyr Khilya. "4-(1-Oxo-1H-isochromen-3-yl)benzenesulfonamides and their effect on cancer cell growth." Ukrainica Bioorganica Acta 16, no. 2 (2021): 30–33. http://dx.doi.org/10.15407/bioorganica2021.02.030.

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Sulfonamide derivatives of 3-phenyl-1H-isochromen-1-one were synthesized by reaction of 4-(1-oxo-1H-isochromen-3-yl)benzenesulfonyl chloride with amines. The specific parameters of chlorosulfonation of 3-phenyl-1H-isochromen-1-one have been identified; the procedure for synthesis of 4-(1-oxo-1H-isochromen-3-yl)benzenesulfonyl chloride and its by-product (disulfochloride) was optimized. The evaluation of anticancer activity of obtained sulfonamides showed no appreciable cytotoxicity
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2

Hathwar, Venkatesha R., P. Manivel, F. Nawaz Khan, and T. N. Guru Row. "3-Butyl-1H-isochromen-1-one." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): o3707. http://dx.doi.org/10.1107/s1600536807037671.

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3

Shablykin, Oleh V., Olga V. Shablykina, and Ilona Yu Tarasiuk. "Preliminary evaluation of the effect of partially hydrogenated 3-acetylisocoumarin derivatives on the cancer cells growth." Ukrainica Bioorganica Acta 19, no. 2 (2024): 33–36. https://doi.org/10.15407/bioorganica2024.02.033.

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In different conditions, from 3-acetyl-1H-isochromen-1-one three partial reduction products were obtained, namely 3-(1-hydroxyethyl)-1H-isochromen-1-one, 3-(1-hydroxyethyl)isochroman-1-one, and 3-ethylisochroman-1-one. The influence of two products with an alcohol fragment, as well as 4-hydroxy-1,2,3,4-tetrahydro-6H-benzo[c]chromen-6-one, on the growth of cancer cells was investigated through One Doses Full NCI 60 Cell Panel Assay. The only one significant effect was found: 3-(1-hydroxyethyl)-1H-isochromen-1-one practically stops the growth of CCRF-CEM cell lines (Leukemia)
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4

Qadeer, Ghulam, Nasim Hasan Rama, Muhammad Azaad Malik, Javeed Akhtar, and Madeleine Helliwell. "3-(3,4,5-Trimethoxyphenyl)-1H-isochromen-1-one." Acta Crystallographica Section E Structure Reports Online 63, no. 8 (2007): o3447. http://dx.doi.org/10.1107/s1600536807032783.

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5

Ali, Farukh Iftakhar, Tariq Mahmood Babar, Nasim Hasan Rama, and Peter G. Jones. "3-(3-Bromobenzyl)-1H-isochromen-1-one." Acta Crystallographica Section E Structure Reports Online 65, no. 10 (2009): o2511. http://dx.doi.org/10.1107/s1600536809037246.

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6

Abid, Obaid-Ur-Rehman, Ghulam Qadeer, Nasim Hasan Rama, Ales Ruzicka, and Zdenka Padelkova. "3-(3-Chlorobenzyl)-1H-isochromen-1-one." Acta Crystallographica Section E Structure Reports Online 64, no. 10 (2008): o2018. http://dx.doi.org/10.1107/s1600536808030274.

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7

Babar, Tariq Mahmood, Ghulam Qadeer, Obaid-ur-Rahman Abid, Nasim Hassan Rama, and Ales Ruzicka. "3-(3-Fluorobenzyl)-1H-isochromen-1-one." Acta Crystallographica Section E Structure Reports Online 64, no. 12 (2008): o2266. http://dx.doi.org/10.1107/s1600536808035575.

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8

Maiyalagan, T., Venkatesha R. Hathwar, P. Manivel, N. Burcu Arslan, and F. Nawaz Khan. "3-(4-Methoxyphenyl)-1H-isochromen-1-one." Acta Crystallographica Section E Structure Reports Online 65, no. 1 (2008): o128. http://dx.doi.org/10.1107/s1600536808042074.

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9

Shablykina, O. V., O. V. Shablykin, V. V. Ishchenko, A. V. Voronaya, and V. P. Khilya. "Synthesis of 3-hetaryl-1H-isochromen-1-ones based on 3-(2-bromoacetyl)-1H-isochromen-1-one." Chemistry of Heterocyclic Compounds 48, no. 11 (2013): 1621–27. http://dx.doi.org/10.1007/s10593-013-1183-7.

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10

Shablykin, Oleh, Daniil Merzhyievsky, and Olga Shablykina. "The interaction of homophthalic anhydride with (triphenylphosphoranylidene)acetates." French-Ukrainian Journal of Chemistry 5, no. 2 (2017): 62–67. http://dx.doi.org/10.17721/fujcv5i2p62-67.

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In the study of the interaction of homo­phthalic anhydride and methyl (triphenyl­phosphoranylidene)­acetate, along with (1-oxo-1H-isochromen-3‑yl)acetate obtaining, two minor products – (1,3-dioxo-1,2,3,4-tetrahydronaphthalene-2-yl)acetate and 2‑((1‑oxo-1H-isochromen-3-yl)methyl)benzoic acid – had been isolated. The action of tert‑butyl (triphenyl­phosphoranylidene)­acetate on homo­phthalic anhydride didn’t lead to Wittig reaction; the encumbered ylide demonstrated only its basicity, and products of homo­phthalic anhydride self-condensation – 2‑((1‑oxo-1H-isochromen-3-yl)methyl)-benzoic acid a
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