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Journal articles on the topic '5-one'

Author: Grafiati

Published: 7 June 2025

Last updated: 2 August 2025

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1

V., K. Rao. "Synthesis of 4-(5-keto-2-phenyloxazolin-4-ylmethylene)-3-phenylisoxazol-5-one." Journal of Indian Chemical Society Vol. 83, Jan 2006 (2006): 87–88. https://doi.org/10.5281/zenodo.5816494.

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Division of Plant Physiology & Biochemistry, Indian Institute of Horticultural Research. Hessaraghatta. Bangalore-560 089, India <em>E-mail</em> : vkr5@yahoo.com <em>Manuscript received 29 June 2001. revised 4 July 2005. accepted 9 September 2005</em> 3-Phenylisoxazol-5-one (1) reacts with hippuric acid and ethyl orthoformate in acetic anhydride to give 4-(5- keto-2-phenyloxazolin-4-ylmethylene)-3-phenylisoxazol-5-one (4) in a single step.

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2

Rettenbacher, Arno S., and Joachim G. Schantl. "5-Methyl-5-nitrosohexan-2-one, reexamined." Arkivoc 2001, no. 5 (2001): 36–41. http://dx.doi.org/10.3998/ark.5550190.0002.505.

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3

Abid, Obaid-ur-Rahman, Ghulam Qadeer, Nasim Hasan Rama, and Wai-Yeung Wong. "5-Methoxyindan-1-one." Acta Crystallographica Section E Structure Reports Online 63, no. 1 (2006): o165—o166. http://dx.doi.org/10.1107/s1600536806052135.

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4

Chen, Kew-Yu, Tzu-Chien Fang, and Ming-Jen Chang. "5-Hydroxyindan-1-one." Acta Crystallographica Section E Structure Reports Online 67, no. 4 (2011): o992. http://dx.doi.org/10.1107/s1600536811010956.

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5

GROUNDWATER, P. W., and M. A. MUNAWAR. "ChemInform Abstract: Synthesis of 2-Phenyl-4,5,6,7-tetrahydroindol-5-one, -tetrahydrobenzo( b)thiophen-5-one and -tetrahydrobenzo(b)furan-5-one." ChemInform 27, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.199641043.

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6

Ichitani, Masaki, Soh-ichi Kitoh, Shuhei Fujinami, Mitsuhiro Suda, Mitsunori Honda, and Ko-Ki Kunimoto. "5-Isopropyl-5-methyl-2-sulfanylideneimidazolidin-4-one." Acta Crystallographica Section E Structure Reports Online 69, no. 6 (2013): o953. http://dx.doi.org/10.1107/s1600536813013639.

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7

Yathirajan, Hemmige S., Basavegowda Nagaraj, Santhosh L. Gaonkar, Rajenahally S. Narasegowda, Padmarajaiah Nagaraja, and Michael Bolte. "5-Bromo-3H-isobenzofuran-1-one (5-bromophthalide)." Acta Crystallographica Section E Structure Reports Online 61, no. 2 (2005): o345—o346. http://dx.doi.org/10.1107/s160053680500084x.

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8

Yathirajan, Hemmige S., Basavegowda Nagaraj, Santhosh L. Gaonkar, Rajenahally S. Narasegowda, Basappa Prabhuswamy, and Michael Bolte. "5-Amino-3H-isobenzofuran-1-one (5-aminophthalide)." Acta Crystallographica Section E Structure Reports Online 61, no. 2 (2005): o343—o344. http://dx.doi.org/10.1107/s1600536805000851.

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9

Wang, Si Hong, Guan Rong Tian, and Jie Ma. "One‐Pot Synthesis of 5‐Alkylfuran‐2(5H)‐ones." Synthetic Communications 36, no. 9 (2006): 1229–33. http://dx.doi.org/10.1080/00397910500514493.

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10

Palysaeva, Nadezhda V., Nadezhda S. Boltacheva, Pavel A. Slepukhin, et al. "Step by step and one-pot syntheses of 5-hydroxy-5-(polyfluoroalkyl)isoxazol-4(5 H )-one oximes." Mendeleev Communications 28, no. 2 (2018): 126–27. http://dx.doi.org/10.1016/j.mencom.2018.03.003.

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11

Ohno, Y., Y. Akutsu, M. Arai, M. Tamura, T. Matsunaga, and M. Iida. "1H-Tetrazol-5(4H)-one." Acta Crystallographica Section C Crystal Structure Communications 54, no. 8 (1998): 1160–62. http://dx.doi.org/10.1107/s0108270198002108.

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12

Hsu, Tzu-Fang, Yan-Ru Chen, Bor-Hunn Huang, and Ming-Jen Chen. "5-(Diphenylmethylidene)pyrrolidin-2-one." Acta Crystallographica Section E Structure Reports Online 68, no. 11 (2012): o3224. http://dx.doi.org/10.1107/s1600536812043851.

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13

Yathirajan, H. S., B. Narayana, B. V. Ashalatha, B. K. Sarojini, and Michael Bolte. "5-Bromopyrimidin-2(1H)-one." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o923—o924. http://dx.doi.org/10.1107/s1600536807003054.

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14

Khan, Mohd Shaheen, Othman Sulaiman, Rokiah Hashim, Ching Kheng Quah, and Hoong-Kun Fun. "Cholest-5-en-7-one." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1668. http://dx.doi.org/10.1107/s1600536810021598.

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15

Ma, Guo-Chun, Hui-Min Liu, and Wen-Qin Zhang. "5-Ethoxy-5-(1-hydroxyethyl)-1-methylpyrrolidin-2-one." Acta Crystallographica Section E Structure Reports Online 60, no. 9 (2004): o1541—o1542. http://dx.doi.org/10.1107/s1600536804019026.

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16

Deepak, Kumar Kashyap, Deshwar Kushwaha Narva, Sharma Renu, Thakare Manoj, and Srivastav Mahesh. "A facile and one pot highly efficient synthesis of 1,3-oxathiolan-5-one derivatives." Journal of Indian Chemical Society Vol. 92, Jul 2015 (2015): 1133–36. https://doi.org/10.5281/zenodo.5607229.

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Department of Chemistry, NIMS University, Sobha Nagar, Jaipur-303 121, Rajasthan, India <em>E-mail </em>: deepakkashyap601@gmail.com, ashima560@gmail.com Department of Chemistry, Meerut College, Meerut-250 001, Uttar Pradesh, India <em>Manuscript received online 05 October 2014, accepted 21 October 2014</em> An efficient and effective method for the synthesis of 1,3-oxathiolan-5-one derivatives by cyclocondensation reaction at room temperature has been described. This method is an excellent way to obtain the title compounds in quantitative yields in a simple and cost effective way. Applying th

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17

Ablajan, Keyume, та Hainimu Xiamuxi. "Efficient One-Pot Synthesis of β-Unsaturated Isoxazol-5-ones and Pyrazol-5-ones Under Ultrasonic Irradiation". Synthetic Communications 42, № 8 (2011): 1128–36. http://dx.doi.org/10.1080/00397911.2010.535949.

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18

Yagi, Kazuo, Akira Numata, Norihiko Mimori, Toshiro Miyake, Kazutaka Arai, and Shigeru Ishii. "Synthesis and insecticidal activity of novel 1,3,4-oxadiazolin-5-one and pyrazolin-5-one derivatives." Pesticide Science 55, no. 2 (1999): 161–65. http://dx.doi.org/10.1002/(sici)1096-9063(199902)55:2<161::aid-ps881>3.0.co;2-m.

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19

Wang, Ke-Hu, Yulai Hu, Jianglong Wang, et al. "Tin-Powder-Promoted One-Pot Synthesis of 5-Trifluoromethyl-5-aryl-3-methylidenepyrrolidin-2-ones." Synthesis 50, no. 09 (2018): 1907–13. http://dx.doi.org/10.1055/s-0036-1591909.

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A simple and efficient synthetic approach is reported for the synthesis of 5-trifluoromethyl-5-aryl-3-methylidenepyrrolidin-2-ones in moderate to excellent yields via an acid-catalyzed one-pot multicomponent reaction of aromatic trifluoromethyl ketones, acylhydrazines, and ethyl 2-(bromomethyl)acrylate promoted by tin powder. The protocol is operationally simple. The overall process involves allylation and cyclization of the intermediate of acylhydrazones.

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20

Espeland, Ludvik O., and Leiv K. Sydnes. "5-Diethoxymethyl-1,1-diethoxy-5-hydroxyundeca-3,6-diyn-2-one." Molbank 2024, no. 4 (2024): M1896. http://dx.doi.org/10.3390/m1896.

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As an extension of our study of the reactivity of derivatives of 3,3,4,4-tetraethoxybut-1-yne, attempts have been made to achieve acid-catalyzed deacetalization of the diethoxymethyl moieties in 5-diethoxymethyl-1,1,2,2-tetraethoxyundeca-3,6-diyn-5-ol. That was not achieved; instead, only deketalization occurred and afforded the title compound, indicating that the triple bond activates the propargylic diethoxy moiety relative to the other acetal groups.

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21

Fun, Hoong-Kun, Suchada Chantrapromma, Avijit Kr Adak, Annada C. Maity, and Shyamaprosad Goswami. "5-Bromo-5-bromomethyl-2-phenoxy-1,3,2-dioxaphosphorinan-2-one." Acta Crystallographica Section E Structure Reports Online 64, no. 11 (2008): o2228—o2229. http://dx.doi.org/10.1107/s1600536808033631.

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22

Khan, Mohd Shaheen, Othman Sulaiman, Rokiah Hashim, Madhukar Hemamalini та Hoong-Kun Fun. "3β-Chlorocholest-5-en-7-one". Acta Crystallographica Section E Structure Reports Online 66, № 3 (2010): o688. http://dx.doi.org/10.1107/s1600536810006380.

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23

Phillips, Oludotun A., and Leyla H. Sharaf. "5-Hydroxymethyl-oxazolidin-2-one antibacterials." Expert Opinion on Therapeutic Patents 19, no. 4 (2009): 529–40. http://dx.doi.org/10.1517/17530050902800142.

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24

deVal Josè Eduardo, Matè‐Sánchez, and Rafael Maté‐Sánchez deVal. "5 years of One‐time therapy." Clinical Oral Implants Research 30, S19 (2019): 253. http://dx.doi.org/10.1111/clr.209_13509.

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25

Zhang, Zhenfeng, Shuo Jin, Siqian Wang, Bo Liu, and Jianping Guo. "3-Methyl-3-pyrazolin-5-one." Acta Crystallographica Section E Structure Reports Online 60, no. 2 (2004): o315—o316. http://dx.doi.org/10.1107/s160053680302974x.

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26

Crockett, Rowena, Alexander R. Forrester, and R. Alan Howie. "1,4-Diacetyl-1,2,4-triazolin-5-one." Acta Crystallographica Section E Structure Reports Online 60, no. 3 (2004): o460—o461. http://dx.doi.org/10.1107/s1600536804004027.

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27

MacCallum, Catriona J. "Why ONE Is More Than 5." PLoS Biology 9, no. 12 (2011): e1001235. http://dx.doi.org/10.1371/journal.pbio.1001235.

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28

Conti, Diego. "Cohomogeneity One Einstein-Sasaki 5-Manifolds." Communications in Mathematical Physics 274, no. 3 (2007): 751–74. http://dx.doi.org/10.1007/s00220-007-0286-3.

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29

Yuan, Mao-Sen, Qi Shuai, Lin Wang, Xiao-Zhou Li, and Rui-Jin Yu. "5-Bromo-1-methylindolin-2-one." Acta Crystallographica Section E Structure Reports Online 65, no. 7 (2009): o1553. http://dx.doi.org/10.1107/s1600536809021564.

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30

Sha, Fei, Hao Xu, Shan Liu, Peng Wang, and Jin-tang Wang. "1-Benzyl-1,4-diazepan-5-one." Acta Crystallographica Section E Structure Reports Online 64, no. 3 (2008): o569. http://dx.doi.org/10.1107/s1600536808001773.

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31

Finch, Arthur, P. J. Gardner, A. J. Head, and H. S. Majdi. "The enthalpies of formation of 1,2,4-triazol-5-one and 3-nitro-1,2,4-triazol-5-one." Journal of Chemical Thermodynamics 23, no. 12 (1991): 1169–73. http://dx.doi.org/10.1016/s0021-9614(05)80150-8.

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32

Nan'ya, Seiko, Eturô Maekawa, Wen-Bing Kang, and Yoshio Ueno. "Synthesis of 11-aza-5H-benzophenoxazin-5-one and 11-Aza-5H-pyridophenoxazin-5-one derivatives." Journal of Heterocyclic Chemistry 23, no. 6 (1986): 1697–700. http://dx.doi.org/10.1002/jhet.5570230619.

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33

Kuhn, Norbert, Cäcilia Maichle-Mößmer, Manfred Steimann, Isabel Walker, and Klaus-Peter Zeller. "1,3-Dialkyl-5-hydroxy-2-thioxoimidazolidin-4-one / 1,3-Dialkyl-5-hydroxy-2-thioxoimidazolidin-4-ones." Zeitschrift für Naturforschung B 65, no. 4 (2010): 533–36. http://dx.doi.org/10.1515/znb-2010-0417.

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The 1,3-dialkyl-5-hydroxy-2-thioxoimidazolidin-4-ones 8 (R = Me, Et, iPr) were obtained from the corresponding thiourea and glyoxylic acid monohydrate in very good yield. Their reactions with chlorotrimethylsilane in the presence of triethylamine gave the 1,3-dialkyl-5-trimethylsiloxy-2-thioxoimidazolidin- 4-ones 9. NMR and crystal structure data of 1,3-diisopropyl-5-hydroxy-4-thioxoimidazolidin-4-one (8c) have confirmed the acyloin-type structure of the above mentioned compounds.

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34

Arfaoui, Aïcha, Imen Beltaïef, and Hassen Amri. "One-Pot Synthesis of [1,2]Isoxazolidin-5-ones and [1,2]Oxazin-6-ones." Synthetic Communications 41, no. 10 (2011): 1536–43. http://dx.doi.org/10.1080/00397911.2010.487292.

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35

Ablajan, Keyume, та Hainimu Xiamuxi. "ChemInform Abstract: Efficient One-Pot Synthesis of β-Unsaturated Isoxazol-5-ones and Pyrazol-5-ones under Ultrasonic Irradiation." ChemInform 43, № 36 (2012): no. http://dx.doi.org/10.1002/chin.201236029.

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36

Xie, Mei, and W. J. Le Noble. "Stereochemistry of reduction and methylation of 5-(trimethylsilyl)adamantan-2-one and 5-(trimethylstannyl)adamantan-2-one." Journal of Organic Chemistry 54, no. 16 (1989): 3836–39. http://dx.doi.org/10.1021/jo00277a018.

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37

Yagi, Kazuo, Akira Numata, Norihiko Mimori, Toshiro Miyake, Kazutaka Arai, and Shigeru Ishii. "Synthesis and insecticidal activity of novel 1, 3, 4-oxadiazolin-5-one and pyrazolin-5-one derivatives." Pesticide Science 55, no. 2 (1999): 161–65. http://dx.doi.org/10.1002/ps.2780550208.

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38

Saint-Loup, René, Jean-Jacques Robin, and Bernard Boutevin. "Synthesis of a Liquid Bisoxazolin-5-one by Radical Reaction of Bismercaptan onto 2-Ethenyloxazolin- 5-one." Macromolecular Chemistry and Physics 203, no. 1 (2002): 199–211. http://dx.doi.org/10.1002/1521-3935(20020101)203:1<199::aid-macp199>3.0.co;2-l.

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39

Kubicki, Maciej. "Two tautomers in one crystal: 4(5)-nitro-5(4)-methoxyimidazole." Acta Crystallographica Section B Structural Science 60, no. 2 (2004): 191–96. http://dx.doi.org/10.1107/s0108768104003179.

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The case of prototropic annular tautomerism in an imidazole derivative has been found. The crystal structure contains a 50:50 mixture of two tautomers: 4-nitro-5-methoxyimidazole and 5-nitro-4-methoxyimidazole. The X-ray experiment actually shows the superposition of these compounds; it appears as if the structure is centrosymmetric and the N—H hydrogen atoms are disordered over two ring N atoms. Owing to the hydrogen-bond pattern, the values of their site occupation factors have to be exactly equal to 1/2. The molecules are connected into a three-dimensional network by means of N—H...N and C—

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40

Gao, Yan-Jiao, Yu-Huang Wang, and Jian-Liang Ye. "1-Benzyl-5-ethyl-5-hydroxy-1H-pyrrol-2(5H)-one." Acta Crystallographica Section E Structure Reports Online 69, no. 7 (2013): o1136. http://dx.doi.org/10.1107/s1600536813016887.

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41

I., R. TREHAN, SINGH LABH, SINGH VASUNDHARA, and L. KAD G. "A Short Synthesis of Undecan-3-one, 5-Methyl-5(E)-hepten-2-one and 4,6-Dimethyl-6(E)-nonen-3-one." Journal of Indian Chemical Society Vol. 74, June 1997 (1997): 500–501. https://doi.org/10.5281/zenodo.5882305.

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Department of Chemistry , Panjab University, Chandigarh-160 014 Manuscript received 29 December 1995, accepted 11 April 1996 A Short Synthesis of Undecan-3-one, 5-Methyl-5(E)-hepten-2-one and 4,6-Dimethyl-6(E)-nonen-3-one  

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42

Brehm, Lotte, Jørgen S. Johansen, and Povl Krogsgaard-Larsen. "Isoxazol-5(4H)-ones. X-Ray crystal structures of a 4-hydroxyisoxazol-5(4H)-one and a [4,4′-biisoxazole]-5(4H),5′(4′H)-dione formed by oxygen oxidation of 3-tert-butyl-4-methylisoxazol-5(4H)-one." J. Chem. Soc., Perkin Trans. 1, no. 16 (1992): 2059–63. http://dx.doi.org/10.1039/p19920002059.

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43

Terashima, Shiro, Noriyuki Nakajima, Masayuki Kirihara, Miyoko Matsumoto, Masaru Hashimoto, and Tadashi Katoh. "One-Step Synthesis of (-)-5-epi-Hydantocidin." HETEROCYCLES 42, no. 2 (1996): 503. http://dx.doi.org/10.3987/com-95-s79.

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44

Hossain, Md Zahangir, Partha Pratim Dey, and M. Asifuzzaman. "One-error correcting [5, 2] ternary codes." Journal of Discrete Mathematical Sciences and Cryptography 22, no. 6 (2019): 935–41. http://dx.doi.org/10.1080/09720529.2019.1624337.

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45

Wawrzak, Z., P. Grochulski, and Z. Gałdecki. "Structure of cholest-5-en-4-one." Acta Crystallographica Section C Crystal Structure Communications 47, no. 3 (1991): 687–89. http://dx.doi.org/10.1107/s0108270190009088.

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46

Grochulski, P., Z. Wawrzak, and Z. Gałdecki. "Structure of cholest-5-en-3-one." Acta Crystallographica Section C Crystal Structure Communications 47, no. 3 (1991): 682–84. http://dx.doi.org/10.1107/s0108270190009155.

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47

Liu, Yuan-Yuan, Hong Shi, Qing-Yan Chu, and Hong-Jun Zhu. "5-(3-Fluorophenyl)-1-phenylpyrazolidin-3-one." Acta Crystallographica Section E Structure Reports Online 64, no. 10 (2008): o1886. http://dx.doi.org/10.1107/s1600536808026706.

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48

Shi, Hong, Hong-Jun Zhu, Peng-Wei Yin, Jin-Tang Wang, and Xiao-Lan Shi. "5-(4-Methoxyphenyl)-1-phenylpyrazolidin-3-one." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): o2246—o2247. http://dx.doi.org/10.1107/s1600536805019227.

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49

Martins, Marcos A. P., Rogério Freitag, Alex F. C. Flores, and Nilo Zanatta. "One-Pot Synthesis of 3(5)-Ethoxycarbonylpyrazoles." Synthesis 1995, no. 12 (1995): 1491–92. http://dx.doi.org/10.1055/s-1995-4147.

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50

Blaskovich, Mark A., and Michael Kahn. "Mild Conditions for Oxazolidin-5-one Formation." Synthesis 1998, no. 04 (1998): 379–80. http://dx.doi.org/10.1055/s-1998-4486.

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