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Journal articles on the topic '5-hydroxy-3'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Fang, Mei-Juan, Hua Fang, Zan-Bin Wei, Dan-Qing Pei, and Yu-Fen Zhao. "Methyl 2-(2-carboxy-3-hydroxy-5-methylphenoxy)-5-hydroxy-3-methoxybenzoate." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o894—o895. http://dx.doi.org/10.1107/s1600536807002280.

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2

ZELENIN, K. N., I. P. BEZHAN, and I. V. LAGODA. "ChemInform Abstract: 5(3)-Hydroxy-3(5)-isoxazolidinones and 5-Hydroxy-3-pyrazolidinones and Their Ring-Chain Tautomerism." ChemInform 23, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199208206.

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3

Żądło-Dobrowolska, Anna, Joerg H. Schrittwieser, Barbara Grischek, Dominik Koszelewski, Wolfgang Kroutil, and Ryszard Ostaszewski. "A convenient stereoselective synthesis of 5-hydroxy-3-oxoesters and 3-hydroxy-5-oxoesters." Tetrahedron: Asymmetry 28, no. 6 (2017): 797–802. http://dx.doi.org/10.1016/j.tetasy.2017.05.005.

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4

Unangst, Paul C., David T. Connor, and Steven R. Miller. "Synthesis of novel 5-hydroxy-3-alkoxy- and 5-hydroxy-3-alkylthioindole-2-carboxamides." Journal of Heterocyclic Chemistry 33, no. 6 (1996): 1627–30. http://dx.doi.org/10.1002/jhet.5570330614.

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5

Han, You-Yue, Yong-Hong Li, and Qiu-Rong Zhao. "2-Hydroxy-N′-(2-hydroxy-3-methoxy-5-nitrobenzylidene)-3-methylbenzohydrazide." Acta Crystallographica Section E Structure Reports Online 66, no. 5 (2010): o1084. http://dx.doi.org/10.1107/s1600536810012912.

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6

Stoermer, Martin, and John Pinhey. "Ethyl 3-Hydroxy-3-methyl-5-phenylpentanoate." Molecules 3, no. 8 (1998): M59. http://dx.doi.org/10.3390/m59.

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7

Stoermer, Martin, and John Pinhey. "3-Hydroxy-3-methyl-5-phenylpentanoic Acid." Molecules 3, no. 8 (1998): M61. http://dx.doi.org/10.3390/m61.

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8

Xue, Rui-Ting, and Mei-Ju Niu. "2-Hydroxy-5-(2-hydroxy-3-methoxybenzylideneamino)benzoic acid." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): o3812. http://dx.doi.org/10.1107/s1600536807036768.

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9

Yang, De-Suo. "3-Hydroxy-N′-(5-hydroxy-2-nitrobenzylidene)-2-naphthohydrazide." Acta Crystallographica Section E Structure Reports Online 65, no. 12 (2009): o2978. http://dx.doi.org/10.1107/s1600536809045279.

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10

Zhu, Zhao-Fu, Li-Juen Shao, and Xi-Hai Shen. "2-Hydroxy-N′-(5-hydroxy-2-nitrobenzylidene)-3-methylbenzohydrazide." Acta Crystallographica Section E Structure Reports Online 68, no. 3 (2012): o559. http://dx.doi.org/10.1107/s1600536812002437.

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11

Lu, Jiu-Fu, Suo-Tian Min, Hong-Guang Ge, Xiao-Hui Ji, and Yue-Fei Bai. "N′-(5-Bromo-2-hydroxy-3-methoxybenzylidene)-4-hydroxy-3-methoxybenzohydrazide dihydrate." Acta Crystallographica Section E Structure Reports Online 65, no. 9 (2009): o2259. http://dx.doi.org/10.1107/s1600536809033522.

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12

Babu, Sainath, Achuthan C. Raghavamenon, Frank R. Fronczek, and Rao M. Uppu. "4-Hydroxy-3-methoxy-5-nitroacetophenone (5-nitroapocynin)." Acta Crystallographica Section E Structure Reports Online 65, no. 9 (2009): o2292—o2293. http://dx.doi.org/10.1107/s160053680903390x.

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13

Zhou, Qing-Li, Chang-Lu Wang, and Zuo-Liang Jing. "4-Hydroxy-3-iodo-5-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 63, no. 6 (2007): o2795. http://dx.doi.org/10.1107/s1600536807020983.

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14

Gunasekaran, B., A. Jayamani, N. Sengottuvelan, and G. Chakkaravarthi. "2-Hydroxy-3-methoxymethyl-5-methylbenzaldehyde." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (2013): o317. http://dx.doi.org/10.1107/s1600536813002845.

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15

UNANGST, P. C., D. T. CONNOR, and S. R. MILLER. "ChemInform Abstract: Synthesis of Novel 5-Hydroxy-3-alkoxy- and 5-Hydroxy-3-alkylthioindole- 2-carboxamides." ChemInform 28, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199725108.

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16

Nosova, N. V., A. V. Vagapov, V. L. Gein, L. F. Gein, and P. A. Slepukhin. "Synthesis and Structure of 3-Aryl-2,4-dibenzoyl-5-hydroxy-5-methylcyclohexanones and 2-Benzoyl-5-hydroxy-5-methyl-3-phenylcyclohexanone." Russian Journal of General Chemistry 88, no. 5 (2018): 903–7. http://dx.doi.org/10.1134/s1070363218050109.

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17

Fujiwara, Kenshu, Misa Tsunashima, Daisuke Awakura, and Akio Murai. "Synthesis of 3-Hydroxy-5-oxonenevia2,3-Epoxy-5-oxonene." Chemistry Letters 26, no. 7 (1997): 665–66. http://dx.doi.org/10.1246/cl.1997.665.

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18

Ye, Jia, Ya-Nan Liu, and Yu Cheng. "Methyl 5-hydroxy-3-phenyl-1,2-oxazolidine-5-carboxylate." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (2012): o1537. http://dx.doi.org/10.1107/s1600536812017576.

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19

Usova, Elena, Ludmila Lysenko, and Gennady Krapivin. "2-Ethoxycarbonyl-3-(2-furyl)-5-hydroxy-5-methylcyclohexanone." Molecules 5, no. 12 (2000): M127. http://dx.doi.org/10.3390/m127.

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20

Rijal, Chairul, Winarto Haryadi, and Chairil Anwar. "Synthesis of Chalcone Derivatives from Halogenated Vanillin and their Activity Test as Antioxidant." Materials Science Forum 1061 (May 26, 2022): 59–65. http://dx.doi.org/10.4028/p-5k5d4j.

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Synthesis of 3-chloro-4-hydroxy-5-methoxybenzaldehyde, 3-bromo-4-hydroxy-5-methoxybenzaldehyde and 2',4'-dihydroxy-3-bromo-4-hydroxy-5-methoxyhalcone and evaluation of their antioxidant activity have been carried out. 3-Chloro-4-hydroxy-5-methoxybenzaldehyde was obtained through chlorination of vanillin using Ca(ClO)2, while 3-bromo-4-hydroxy-5-methoxybenzaldehyde was obtained via bromination of vanillin using KBrO3 in glacial acetic acid solvent and 47% HBr catalyst. Then, 2',4'-dihydroxy-3-bromo-4-hydroxy-5-methoxychalcone was prepared from 3-bromo-4-hydroxy-5-methoxybenzaldehyde and 2-4-dih

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21

Karadayı, Nevzat, Çiğdem Albayrak, Mustafa Odabaşoğlu, and Orhan Büyükgüngör. "(E)-5-[(3-Chlorophenyl)diazenyl]-2-hydroxy-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): o1699—o1701. http://dx.doi.org/10.1107/s1600536806009858.

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The title compound, C14H11ClN2O3, contains an azo group (–N=N–), and the configuration around the –N=N– double bond is trans. There are intramolecular O—H...O and intermolecular C—H...O hydrogen bonds, and the crystal packing is stabilized by C—H...π and π–π stacking interactions, forming a two-dimensional network.

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22

Şahin, Onur, Çigˇdem Albayrak, Mustafa Odabaşogˇlu, and Orhan Büyükgüngör. "(E)-5-[(3-Bromophenyl)diazenyl]-2-hydroxy-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 12 (2005): o4276—o4278. http://dx.doi.org/10.1107/s1600536805038365.

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23

Khanum, S. A., M. Mahendra, S. Shashikanth, B. H. Doreswamy, M. A. Sridhar, and J. Shashidhara Prasad. "(3-Chlorophenyl)(2-hydroxy-5-methylphenyl)methanone." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3615—o3617. http://dx.doi.org/10.1107/s1600536805031776.

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24

Chinnakali, K., K. Sivakumar, S. Natarajan, M. N. Ponnuswamy, and E. W. Czerwinski. "3-(2-Hydroxy-5-methylbenzyl)-6-methylcoumarin." Acta Crystallographica Section C Crystal Structure Communications 47, no. 2 (1991): 330–32. http://dx.doi.org/10.1107/s0108270190003274.

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25

Jedrzejas, M. J., M. Luo, S. Singh, W. J. Brouillette, and G. M. Air. "4-(Acetylamino)-3-hydroxy-5-nitrobenzoic Acid." Acta Crystallographica Section C Crystal Structure Communications 51, no. 9 (1995): 1910–12. http://dx.doi.org/10.1107/s0108270195003258.

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26

Chen, Yuting, Da-Cheng Li, Yuehua Zhu, and Da-Qi Wang. "5-Hydroxy-1-(3-hydroxy-2-naphthoyl)-3,5-dimethyl-2-pyrazoline." Acta Crystallographica Section E Structure Reports Online 64, no. 8 (2008): o1629. http://dx.doi.org/10.1107/s1600536808023027.

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27

Prager, RH, and JA Smith. "The Chemistry of 5-Oxodihydroisoxazoles. XI. The Photolysis of 3-Hydroxy-4-phenylisoxazol-5(2H)-ones (Phenyldisic Acids)." Australian Journal of Chemistry 48, no. 2 (1995): 217. http://dx.doi.org/10.1071/ch9950217.

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3-Hydroxy-2-methyl-4-phenylisoxazol-5(2H)-one, 3-hydroxy-2,4-diphenylisoxazol-5(2H)-one and phenyldisic acid have been photolysed at 254 nm in hydroxylic solvents. By comparison of the respective products with those obtained from 3-methoxy-4-phenylisoxazol- 5(2H)-one, 5-methoxy-4-phenylisoxazol-3(2H)-one and 5(3)-hydroxy-2,2-dimethyl-3(5)-oxo-4-phenyldihydroisoxazolium hydroxide, it is apparent that the disic acids photolyse independently from the 3-hydroxy 5-one, the 5-hydroxy 3-one and the zwitterion tautomers. Novel photochemical pathways for these processes are suggested.

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28

Ishani, Isita, and T. Vijayakumar. "Exploitation of Versatile Naturally Derived Blue Colorant Pigment 3-[2-hydroxy-5-(5-hydroxy-1H-indol-3-yl)-1H-pyrrol-3-yl] indol-one." IOP Conference Series: Materials Science and Engineering 1219, no. 1 (2021): 012020. http://dx.doi.org/10.1088/1757-899x/1219/1/012020.

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Abstract 3-[2-hydroxy-5-(5-hydroxy-1H-indol-3-yl)-1H-pyrrol-3-yl] indol-one depicts a multifaceted pigment which was discovered in distinct bacteria species like Chromobacterium violaceum, Duganella sp. , Collimonas sp. , D. violaceinigra , Pseudoalteromonas sp. , J. svalbardensis , Janthinobacteriumlividum, etc. 3-[2-hydroxy-5-(5-hydroxy-1H-indol-3-yl)-1H-pyrrol-3-yl] indol-one is liable for the stunning purple pastels which demonstrates a variety of biological behaviors and is reportedly garnering growing popularity in industrial- market segments, for instance, textiles, medicine, cosmetics

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29

Journal, Baghdad Science. "Synthesized azodyes of 2-amino-1, 3, 4- thiadiazole - 5 - thiol." Baghdad Science Journal 8, no. 2 (2011): 269–73. http://dx.doi.org/10.21123/bsj.8.2.269-273.

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Several azo dyes were synthesized through coupling reaetion of some substituted phenols and B.naphthol with diazonium salt of 2- amino-1,3-4- thiadiazol -5- thiol. All the synthesized compounds during this work were characterized using some speetral data (F.TIRand UV)andM.P . 2-[4 --Hydroxy napthyl-azo ] -1,3,4-Thiadiazol -5-Thiol • 2- [2-- hydroxy –4- NO2 – phenyl- azo]- 1,3,4 - Thiadiazol –5-Thiol. • 2- [3--Amino-4-Hydroxy phenyl –azo]-1,3,4 - Thiadiazol –5-Thiol. . • 2-[2--Amino-4-Hydroxy phenyl -azo]-1,3,4 - Thiadiazol –5-Thiol . • 2- [3--Amino-6- Hydroxy phenyl -azo]-1,3,4 - Thiadiazol –5

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30

Ge, Yan-Qing, Wen-Liang Dong, Yong Xia, Fang Wei, and Bao-Xiang Zhao. "Ethyl 3-(2-hydroxy-5-methylphenyl)-1H-pyrazole-5-carboxylate." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): o1313—o1314. http://dx.doi.org/10.1107/s1600536807006745.

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The non-H atoms of the title molecule, C13H14N2O3, are approximately coplanar. The molecules are linked into a two-dimensional network parallel to the bc plane by intermolecular N—H...O, C—H...O and C—H...π interactions.

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31

Bolte, M. "1-Benzoyl-5-hydroxy-2,4-diphenyl-5-propionyloxy-3-imidazoline." Acta Crystallographica Section C Crystal Structure Communications 53, no. 12 (1997): IUC9700027. http://dx.doi.org/10.1107/s0108270197099290.

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32

MANZ, B., G. SCHÜLER, and K. POLLOW. "Radioimmunoassay of urinary 5-hydroxy-3-indoleacetic acid (5-HIAA)." Acta Endocrinologica 113, no. 1_Suppl (1986): S206—S207. http://dx.doi.org/10.1530/acta.0.111s206.

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33

Asiri, Abdullah M., Abdulrahman O. Al-Youbi, Hassan M. Faidallah, and Seik Weng Ng. "5-Hydroxy-3-phenyl-5-trifluoromethyl-4,5-dihydro-1H-pyrazole." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2442. http://dx.doi.org/10.1107/s160053681103368x.

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34

Zelenin, K. N., I. P. Bezhan, and I. V. Lagoda. "5(3)-Hydroxyisoxazolidin-3(5)-ones and 5-hydroxy-pyrazolidin-3-ones and their ring-chain tautomerism." Chemistry of Heterocyclic Compounds 27, no. 2 (1991): 232–33. http://dx.doi.org/10.1007/bf00476765.

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35

Shu, Ren-Geng, Hai-Liang Zhu, and Ren-Xiang Tan. "Methyl 5-hydroxy-2-(2-hydroxy-6-methoxy-4-methylbenzoyl)-3-methoxybenzoate." Acta Crystallographica Section E Structure Reports Online 61, no. 1 (2004): o189—o191. http://dx.doi.org/10.1107/s160053680403346x.

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36

Karadayı, Nevzat, Çiğdem Albayrak, Mustafa Odabaşoğlu, and Orhan Büyükgüngör. "(E)-2-Hydroxy-3-methoxy-5-[(3-methoxyphenyl)diazenyl]benzaldehyde." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): o1727—o1729. http://dx.doi.org/10.1107/s1600536806011263.

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The molecule of the title compound, C15H14N2O4, is approximately planar and displays a trans configuration with respect to the N=N double bond. The molecules are linked by intermolecular C—H...O and C—H...π interactions, forming a three-dimensional network.

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37

Chen, Chung-Yi, Yu-Ting Yeh, and Woei-Ling Yang. "New Phenylalkanoids from Zingiber Officinale." Natural Product Communications 6, no. 6 (2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600624.

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Two new phenylalkanoids, 3-hydroxy-1-(4′-hydroxy-3′-methoxy-phenyl)-hexan-5-one (1) and 3-hydroxy-1-(3′, 5′-dimethoxy-4′-hydroxy-phenyl)-hexan-5-one (2) were isolated from the rhizomes of Chinese ginger ( Zingiber officinale Roscoe (Zingiberaceae)). The structures of two new phenylalkanoids were elucidated by chemical and physical evidence.

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38

Zhou, Wei, Zhimin Wu, Weixiao Hu, and Chunnian Xia. "10-(4-Hydroxy-3-methoxy-5-nitrobenzylidene)anthrone." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4498. http://dx.doi.org/10.1107/s1600536807052919.

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In the title compound, C22H15NO5, prepared from anthrone and 4-hydroxy-3-methoxy-5-nitrobenzaldehyde, the anthracene fragment is non-planar. The central six-membered ring assumes an asymmetric boat conformation, while the two outer benzene rings make a dihedral angle of 28.08 (10)°. The hydroxy group is involved in an intramolecular hydrogen bond. In the crystal structure, a weak intermolecular C—H...O hydrogen bond links the molecules into ribbons along the c axis.

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39

Aghamaliyev, Z. Z. "SYNTHESIS OF 2-HYDROXY-3-(METHYLCYCLOHEXENYLISOPROPYL) -5- CHLOROBENZYLAMINOETHYLNONYLIMIDAZOLINES." Chemical Problems 16, no. 2 (2018): 218–22. http://dx.doi.org/10.32737/2221-8688-2018-2-218-222.

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40

Tian, Hong-Yu, Hong-Lin Ye, Bao-Guo Sun, and Ya-Ling Wang. "Synthesis of 2-hydroxy-5-methyl-3-hexanone." Journal of Chemical Research 35, no. 1 (2011): 51–52. http://dx.doi.org/10.3184/174751911x12964930076747.

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41

Peng, San-Jun, and Hai-Yun Hou. "N′-(5-Bromo-2-hydroxy-3-methoxybenzylidene)isonicotinohydrazide." Acta Crystallographica Section E Structure Reports Online 64, no. 10 (2008): o1995. http://dx.doi.org/10.1107/s1600536808029607.

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42

IŞlik, Şamil, Muhittin Aygün, Selami Işaşmaz, et al. "Structure of 5-Allyl-2-hydroxy-3-methoxyazobenzene." Spectroscopy Letters 30, no. 8 (1997): 1525–49. http://dx.doi.org/10.1080/00387019708006742.

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43

Odabaşoğlu, Mustafa, Çiğdem Albayrak, and Orhan Büyükgüngör. "Bis(3-formyl-4-hydroxy-5-methoxyphenyl)methane." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): o239—o240. http://dx.doi.org/10.1107/s1600536805041334.

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44

Kılıç, Işın, Şamil Işık, Erbil Ağar, and Ferda Erşahin. "3-[(2,4-Dichlorophenyl)iminomethyl]-2-hydroxy-5-methylbenzaldehyde." Acta Crystallographica Section E Structure Reports Online 65, no. 6 (2009): o1347. http://dx.doi.org/10.1107/s1600536809018303.

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The title compound, C15H11Cl2NO2, is a Schiff base which adopts the phenol–imine tautomeric form in the solid state, being stabilized by a strong intramolecular O—H...N hydrogen bond. The molecule is almost planar (r.m.s. deviation for all non-H atoms = 0.049 Å), displaying a dihedral angle of 3.1 (3)° between the planes of the two aromatic rings.

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45

Cox, P. J., and R. A. Howie. "Structure of 5-hydroxy-2-methyl-3-[1,2,3,4-tetrahydro-2-(1,4-dihydro-5-hydroxy-2-methyl-1,4-dioxo-3-naphthyl)-5-hydroxy-2-methyl-1,4-dioxo-3-naphthylmethyl]-1,4-naphthoquinone toluene solvate." Acta Crystallographica Section C Crystal Structure Communications 46, no. 7 (1990): 1349–51. http://dx.doi.org/10.1107/s0108270190002281.

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46

J., VIROOPAKSHAPPA, and VITHAL RAO D. "Synthesis and Characterisation of Cobalt(II), Nickel(II) and Copper(II) Chelates of 3-(2-Hydroxy-5-chlorobenzylideneamino)-5-methylisoxazole and 3-(2-Hydroxy- 5-bromobenzylideneamino)-5-methylisoxazole." Journal of Indian Chemical Society Vol. 73, Oct 1996 (1996): 531–32. https://doi.org/10.5281/zenodo.5910404.

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Department of Chemistry, Kakatiya University, Warangal-506 009 <em>Manuscript received  28 December 1993, revised  25 January 1995, accepted 16 February 1995</em> Synthesis and Characterisation of Cobalt(II), Nickel(II) and Copper(II) Chelates of 3-(2-Hydroxy-5-chlorobenzylideneamino)-5-methylisoxazole and 3-(2-Hydroxy- 5-bromobenzylideneamino)-5-methylisoxazole.

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47

Swamy, G. Y. S. K., K. Ravikumar, P. Narender, and V. Jayathirtha Rao. "Ethyl 3-(2-chloro-5-methyl-3-pyridyl)-3-hydroxy-2-methylenepropanoate." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2188—o2189. http://dx.doi.org/10.1107/s1600536807014535.

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48

Swamy, G. Y. S. K., K. Ravikumar, P. Narender, and V. Jayathirtha Rao. "Methyl 3-(2-chloro-5-ethyl-3-pyridyl)-3-hydroxy-2-methylenepropanoate." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1612—o1614. http://dx.doi.org/10.1107/s1600536806010646.

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The molecule of title compound, C12H14ClNO3, has an L-shaped conformation, with the methyl propanoate unit at the base. The molecules are linked via O—H...N hydrogen bonds into infinite chains of graph-set motif C(6) running along the b axis. In addition, the structure is further stabilized by C—H...O, C—H...Cl and C—H...π interactions.

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49

Li Kam Wa, T. C., S. Freestone, R. R. Samson, N. R. Johnson, and M. R. Lee. "A Comparison of the Renal and Neuroendocrine Effects of Two 5-Hydroxytryptamine Renal Prodrugs in Normal Man." Clinical Science 85, no. 5 (1993): 607–14. http://dx.doi.org/10.1042/cs0850607.

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1. The effects of 1 h intravenous infusions of equimolar amounts (45 nmol min−1 kg−1) of two putative 5-hydroxytryptamine renal prodrugs, 5-hydroxy-L-tryptophan and γ-L-glutamyl-5-hydroxy-L-tryptophan, were investigated in a randomized, placebo-controlled, cross-over study in nine healthy male subjects. 2. Cumulative urinary 5-hydroxytryptamine excretion over the 3 h observation period rose by about 370-fold after 5-hydroxy-L-tryptophan and 390-fold after γ-L-glutamyl-5-hydroxy-L-tryptophan when compared with placebo infusion. Urinary 5-hydroxy-L-tryptophan excretion was three times higher aft

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50

Di Nunno, Leonardo, Antonio Scilimati, and Paola Vitale. "5-Hydroxy-3-phenyl-5-vinyl-2-isoxazoline and 3-phenyl-5-vinylisoxazole: synthesis and reactivity." Tetrahedron 61, no. 47 (2005): 11270–78. http://dx.doi.org/10.1016/j.tet.2005.08.077.

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