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1

Benzies, David W. M., Pilar Martinez Fresneda, and R. Alan Jones. "2-Formyl-3-Methoxymethylindole, 3-Ethoxymethyl-2-Formylindole and 2-Formyl-3-Methylindole." Synthetic Communications 16, no. 14 (1986): 1799–807. http://dx.doi.org/10.1080/00397918608057203.

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2

Moreno-Fuquen, Rodolfo, Geraldine Hernandez, Javier Ellena, Carlos A. De Simone, and Juan C. Tenorio. "4-Formyl-2-nitrophenyl 2-chlorobenzoate." Acta Crystallographica Section E Structure Reports Online 69, no. 12 (2013): o1806. http://dx.doi.org/10.1107/s1600536813031346.

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In the title compound, C14H8ClNO5, the benzene rings form a dihedral angle of 19.55 (9)°. The mean plane of the central ester group [r.m.s. deviation = 0.024 Å] forms dihedral angles of 53.28 (13) and 36.93 (16)°, respectively, with the nitro- and chloro-substituted rings. The nitro group forms a dihedral angle of 19.24 (19)° with the benzene ring to which it is attached. In the crystal, molecules are linked by weak C—H...O hydrogen bonds, formingC(7) chains, which run along [100].
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3

Han, Jian-Rong, Xiao-Li Zhen, Xia Tian, and Shou-Xin Liu. "2-(5-Formyl-2-methoxyphenoxy)acetonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5427—o5428. http://dx.doi.org/10.1107/s160053680604640x.

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4

Hu, Qing-Ping, Yan Li, Hong-Yu Zhou, Xiu-Fang Zheng, and Ming-Liang Ma. "5-Formyl-2-methoxyphenyl 2-iodobenzoate." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): o109—o110. http://dx.doi.org/10.1107/s1600536805039978.

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5

Manikandan, N., S. Murugavel, D. Kannan, and M. Bakthadoss. "2-Formyl-6-methoxyphenyl cinnamate." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2167. http://dx.doi.org/10.1107/s160053681202747x.

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6

Moreno-Fuquen, Rodolfo, Geraldine Hernandez, and Alan R. Kennedy. "4-Formyl-2-nitrophenyl benzoate." Acta Crystallographica Section E Structure Reports Online 70, no. 3 (2014): o268. http://dx.doi.org/10.1107/s1600536814002694.

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In the title nitroaryl benzoate derivative, C14H9NO5, the aromatic rings form a dihedral angle of 46.37 (8)°. The central ester moiety, —C—(C=O)—O—, is essentially planar (r.m.s. deviation for all non-H atoms = 0.0283 Å) and forms a dihedral angle of 54.06 (9)° with the 4-formyl-2-nitrophenyl ring and 7.99 (19)° with the benzoate ring. In the crystal, molecules are intertwined by weak C—H...O interactions, forming helical chains along [100].
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7

Zhang, Qiao-Zhen, Yan-Li Zhao, Xin Chen, and Ming Yu. "5-Formyl-2-methoxyphenyl benzenesulfonate." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5711—o5712. http://dx.doi.org/10.1107/s1600536806048938.

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8

Asghar, Muhammad Nadeem, Onur Şahin, Muhammad Nadeem Arshad, Uzma Mazhar, Islam Ullah Khan та Orhan Büyükgüngör. "Poly[[di-μ-aqua-(μ-4-formyl-2-methoxyphenolato)disodium] 4-formyl-2-methoxyphenolate]". Acta Crystallographica Section E Structure Reports Online 66, № 2 (2010): m149—m150. http://dx.doi.org/10.1107/s1600536810000711.

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9

Abe, Noritaka, Kazuya Koizumi, Chikara Miyake, et al. "Syntheses of 2-Formyl-, 2,3-Diformyl- and 8-Formyl-1-azaazulenes." HETEROCYCLES 73, no. 1 (2007): 325. http://dx.doi.org/10.3987/com-07-s(u)6.

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10

Tomas, A., Nguyen Huy Dung, and B. Viossat. "(Formyl-2 pyrrolyl-1)-2 thiophenecarbonitrile-3." Acta Crystallographica Section C Crystal Structure Communications 47, no. 10 (1991): 2222–24. http://dx.doi.org/10.1107/s010827019100358x.

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11

Valencia, Jhesua, Oriel A. Sánchez-Velasco, Jorge Saavedra-Olavarría, Patricio Hermosilla-Ibáñez, Edwin G. Pérez, and Daniel Insuasty. "N-Arylation of 3-Formylquinolin-2(1H)-ones Using Copper(II)-Catalyzed Chan–Lam Coupling." Molecules 27, no. 23 (2022): 8345. http://dx.doi.org/10.3390/molecules27238345.

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3-formyl-2-quinolones have attracted the scientific community’s attention because they are used as versatile building blocks in the synthesis of more complex compounds showing different and attractive biological activities. Using copper-catalyzed Chan–Lam coupling, we synthesized 32 new N-aryl-3-formyl-2-quinolone derivatives at 80 °C, in air and using inexpensive phenylboronic acids as arylating agents. 3-formyl-2-quinolones and substituted 3-formyl-2-quinolones can act as substrates, and among the products, the p-methyl derivative 9a was used as a substrate to obtain different derivatives su
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12

Ishkov, Yurij V., Zinaida I. Zhilina, and Ludmila P. Barday. "The interaction of formylporphyrins with weak CH-acids." Journal of Porphyrins and Phthalocyanines 07, no. 11 (2003): 761–65. http://dx.doi.org/10.1142/s1088424603000938.

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A series of 2(α,β-unsaturated-γ-keto)-5,10,15,20-tetraphenylporphyrins was obtained by condensation of 2-formyl-5,10,15,20-tetraphenylporphyrin with acetone, 1,4-diacetylbenzene, 2-acetylthiophene, acetylacetone and acetophenone according to the Claisen-Schmidt reaction. The condensation product with 1,4-diacetylbenzene could react similarly with another formyl derivative – quinoxalin-6-carboxaldehyde and 2-formyl-5,10,15,20-tetraphenylporphyrin. It is shown that this reaction passes through formation of iminium salt formylporphyrin in presence of free base piperidine and perchloric acid.
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13

Moreno-Fuquen, Rodolfo, Geraldine Hernández, and Alan R. Kennedy. "4-Formyl-2-nitrophenyl 3-nitro-2-methylbenzoate." Acta Crystallographica Section E Structure Reports Online 70, no. 1 (2013): o17. http://dx.doi.org/10.1107/s1600536813032583.

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14

Song, Jun-Song, De-Cai Wang, Xue-Jun He, Jiang-Kai Qiu, and Ping-Kai Ou-yang. "rac-Methyl 2-(2-formyl-4-nitrophenoxy)hexanoate." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (2012): o1395. http://dx.doi.org/10.1107/s1600536812015462.

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15

Moreno-Fuquen, Rodolfo, Geraldine Hernandez, Javier Ellena, Carlos A. De Simone, and Juan C. Tenorio. "4-Formyl-2-nitrophenyl 4-bromobenzoate." Acta Crystallographica Section E Structure Reports Online 69, no. 5 (2013): o793. http://dx.doi.org/10.1107/s1600536813010830.

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16

Ismail, Nor Hadiani, Che Puteh Osman, Khalijah Awang, Sri Nurestri Abdul Malek, and Seik Weng Ng. "2-Formyl-3-hydroxy-9,10-anthroquinone." Acta Crystallographica Section E Structure Reports Online 64, no. 11 (2008): o2164. http://dx.doi.org/10.1107/s1600536808032224.

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17

Guo, Xianghai, Jiaxiang Shen, Liang Wang, and Guangzeng Zhou. "N-Formyl-4-methoxy-2-methylaniline." Acta Crystallographica Section E Structure Reports Online 62, no. 11 (2006): o4862—o4863. http://dx.doi.org/10.1107/s160053680604058x.

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18

Chen, Xin, and Ming Yu. "4-Formyl-2-methoxyphenyl 4-methylbenzenesulfonate." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5775—o5776. http://dx.doi.org/10.1107/s1600536806049221.

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19

Zhang, Qiao-Zhen, Yan-Li Zhao, Xin Chen, and Ming Yu. "5-Formyl-2-methoxyphenyl 4-methylbenzenesulfonate." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): o5889—o5890. http://dx.doi.org/10.1107/s1600536806050653.

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20

Lippmann, Eberhard, and Peter Apel. "Darstellung ven 2-Formyl-4,5-benztropon." Zeitschrift für Chemie 10, no. 11 (2010): 434–35. http://dx.doi.org/10.1002/zfch.19700101107.

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21

SZELL, T., P. SOHAR та GY HORVATH. "ChemInform Abstract: α-Formyl-2-hydroxyacetophenone." ChemInform 27, № 7 (2010): no. http://dx.doi.org/10.1002/chin.199607117.

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22

Ono, Noboru, Emiko Muratani, and Takuji Ogawa. "Preparation of 2-formyl-4-nitropyrroles." Journal of Heterocyclic Chemistry 28, no. 8 (1991): 2053–55. http://dx.doi.org/10.1002/jhet.5570280846.

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23

Sulistyowaty, Melanny Ika, Juni Ekowati, Steven Guitomo, Imamatin Nufus Melania, and Muhammad Ilham Royyan Nafi. "Computational docking toward cox-2 and synthesis of 4-formyl-2-methoxyphenyl-4-chlorobenzoate using microwave irradiation." Pharmacy Education 23, no. 4 (2023): 132–36. http://dx.doi.org/10.46542/pe.2023.234.132136.

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Background: Structure modification of organic compounds is needed to increase their bioactivity. Vanillin has been reported to has various therapeutic effects such as antioxidant, antimutagenic, anti-invasive and metastatic suppression potential, anti-inflammatory and also antinociceptive activity. To increase the activity of organic compounds, we have to enhance the lipophilic properties by modifications of the structure. Objective: The phenolic OH of vanillin can be modified by adding aromatic ring, carbonyl, and halogen to improve its bioactivity. The 4-formyl-2-methoxyphenyl-4-chlorobenzoa
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24

ROSU, Tudor, Angela KRIZA, Viorel CARCU, and Anca NICOLAE. "TRANSITION METAL COMPLEXES OF THE FORMYL VANILLINE DERIVATIVES LIGAND FAMILY." SOUTHERN BRAZILIAN JOURNAL OF CHEMISTRY 5, no. 5 (1997): 67–77. http://dx.doi.org/10.48141/sbjchem.v5.n5.1997.68_1997.pdf.

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Divalent 3d metal complexes with formyl-vanilline derivatives, of lite type ML2 or ML2X2 (M = Cu(II), Co(II); X = Cl), were sythesized by reaction of the corresponding metal(II) chlorides with 1-[3-formyl-4-methoxy-6-hidroxybemilydene]-2-phenazinoyllhydrazine, (FDFH), 1-benzilydene-2-phenazinoyhydrazine, (BFH), and 3-formyl-5,6-dihydroxybemilydenc-2-nitro-1--methylaniline, (FBAH). The novel complexes were characterized by ESR, IR, electronic spectroscopy, molar electric conductibility measurements and magnctk studies. These compounds appear to bn hexacoordinated.
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25

Oliveira, Ana Paula A., Angel A. Recio-Despaigne, Isabella P. Ferreira, et al. "Investigation of the antitrypanosomal effects of 2-formyl-8-hydroxyquinoline-derived hydrazones and their antimony(iii) and bismuth(iii) complexes." New Journal of Chemistry 43, no. 48 (2019): 18996–9002. http://dx.doi.org/10.1039/c9nj02676b.

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2-formyl-8-hydroxyquinoline-4-nitroimidazolhydrazone (H2Q4NO<sub>2</sub>Im, H2La, 1) and 2-formyl-8-hydroxyquinoline-4-nitrobenzenehydrazone (H2Q4NO<sub>2</sub>Ph, H2Lb, 2) were obtained, as well as their Sb(iii) [Sb(L)Cl<sub>2</sub>] (3, 4) and Bi(III) [Bi(L)Cl<sub>2</sub>] (5, 6) complexes.
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26

Li, Xiaoyan, Hongjian Sun, Alexandra Brand, and Hans-Friedrich Klein. "Synthesis of dimethylcobalt(III) complexes containing trimethylphosphine and 2-formyl-phenolato- or 2-formyl-enolato(O:O) ligands." Inorganica Chimica Acta 358, no. 12 (2005): 3329–33. http://dx.doi.org/10.1016/j.ica.2005.05.016.

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27

Klein, Hans-Friedrich, Xiaoyan Li, Ulrich Flörke, and Hans-Jürgen Haupt. "Hydrido(acylenolato)cobalt(III)-Verbindungen mit Trimethylphosphan- Liganden: Insertionsreaktionen mit Alkinen und die ersten Carbonylcobalt(III)-Komplexe / Hydrido(acylenolato)cobalt(III) Compounds Containing Trimethylphosphane Ligands: Insertion Reactions with Alkynes and the First Carbonylcobalt(III) Complexes." Zeitschrift für Naturforschung B 55, no. 8 (2000): 707–17. http://dx.doi.org/10.1515/znb-2000-0807.

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Abstract Formal insertion of phenylethyne into Co-H functions of mer-octahedral acyl(enolato)-cobalt(III) hydrides 1-3 proceeds under ambient conditions affording η1-vinylcobalt(III) compounds where the dianionic acyl(enolato) ligands are derived from 2-formyl-4-phenyl-cyclohexanone (4), 1-formyl-cyclohexan-2-one (5), and 3-hydroxo-2,3-diphenyl-propenal (6). Dissociation and association of trimethylphosphane results in a reversible transformation of penta-coordinate complexes 4 -6 into hexa-coordinate ones 7 -9, respectively, involving different tautomeric vinyl species. In toluene solution 9
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28

Meshulam, T., P. Proto, R. D. Diamond, and D. A. Melnick. "Calcium modulation and chemotactic response: divergent stimulation of neutrophil chemotaxis and cytosolic calcium response by the chemotactic peptide receptor." Journal of Immunology 137, no. 6 (1986): 1954–60. http://dx.doi.org/10.4049/jimmunol.137.6.1954.

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Abstract Stimulation of neutrophils by chemoattractants is followed by a rapid, transient rise in cytosolic calcium concentration. The role of calcium in activation of cell movement and related responses was examined by selectively chelating extracellular or both extra- and intracellular calcium. Removal of calcium from the extracellular medium did not alter the cytosolic calcium concentration (Quin 2 fluorescence, 110 to 120 nM) of unstimulated neutrophils and did not dramatically affect the rise induced by formyl peptide. Despite the intact Quin 2 response, depletion of extracellular calcium
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29

IONITA, Petre. "Synthesis and characterization of a new hydrazyl free radical, a formyl-derivative of DPPH." Revue Roumaine de Chimie 66, no. 2 (2021): 205–9. http://dx.doi.org/10.33224/rrch.2021.66.2.12.

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Starting from 2,2-diphenyl-1-(2,4,6-trinitropheyl)hydrazine and urotropine in the presence of trifluoracetic acid it was obtained a formyl derivative as a yellow solid, that can form under oxidative condition the persistent hydrazyl free radical 2-(p-formyl-phenyl)-2-phenyl-1-(2,4,6-trinitrophenyl)hydrazyl having a violet colour. The same formyl hydrazine derivative in the presence of a base forms the corresponding anion with a red-brown colour. The new compounds were characterized by appropriate means, like NMR, IR, UV-VIS, ESR.
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30

Diao, Chun-Hua, Min-Jie Guo, Ming Yu, Xin Chen, Zuo-Liang Jing, and Qi-Liang Deng. "4-[2-(4-Formyl-2-methoxyphenoxy)ethoxy]-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3741—o3742. http://dx.doi.org/10.1107/s1600536805032861.

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31

Han, Jian-Rong, and Xiao-Li Zhen. "3-[2-(5-Formyl-2-methoxyphenoxy)ethoxy]-4-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3946—o3947. http://dx.doi.org/10.1107/s1600536805035117.

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32

Diao, Chun-Hua, Zhi Fan, Ming Yu, Xin Chen, and Zuo-Liang Jing. "2-[4-(2-Formyl-6-methoxyphenoxy)butoxy]-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 12 (2005): o4067—o4068. http://dx.doi.org/10.1107/s1600536805036317.

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33

Almagro, Luis, Manuel Nogueras, Margarita Suárez, Justo Cobo, and Christopher Glidewell. "Chloro–formyl steroids as precursors for hybrid heterosteroids: synthesis, spectroscopic characterization, and molecular and supramolecular structures." Acta Crystallographica Section C Structural Chemistry 74, no. 12 (2018): 1667–73. http://dx.doi.org/10.1107/s2053229618015887.

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Two new functionalized steroids containing both chloro and formyl substituents in ring A, and intended as precursors for the synthesis of hybrid systems, have been synthesized from ketosteroid precursors. 3-Chloro-2-formyl-17,17-dimethyl-18-nor-5α-androstane-2,13-diene, (I), and methyl 3-chloro-4-formyl-12-oxo-5β-cholan-3-ene-24-oate, C26H37ClO4, (IV), have been synthesized using Vilsmeier reactions with 17β-hydroxy-17α-methyl-5α-androstan-3-one and methyl 3,13-dioxo-5β-cholan-24-oate, respectively. These products have been fully characterized using IR spectroscopy, 1H and 13C NMR spectroscopy
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34

Proksa, Bohumil, Dušan Uhrín, Ján Fuska, and Eva Michálková. "(-)-Mitorubrinol and Phthaldehydic Acids, New Metabolites of Penicillium vermiculatum DANG." Collection of Czechoslovak Chemical Communications 57, no. 2 (1992): 408–14. http://dx.doi.org/10.1135/cccc19920408.

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Three new metabolites - (-)-mitorubrinol, 2-formyl-3,5-dihydroxy-4-methylbenzoic and 2-formyl-3,5-dihydroxy-4-hydroxymethylbenzoic acids - were isolated from the culture medium of Penicillium vermiculatum DANG. Hexane extract of the mycelium contained ergosterol and esters of fatty acids, linoleic, oleic and palmitic acids being the dominating ones.
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35

Vyas, J. M., S. M. Shawar, J. R. Rodgers, R. G. Cook, and R. R. Rich. "Biochemical specificity of H-2M3a. Stereospecificity and space-filling requirements at position 1 maintain N-formyl peptide binding." Journal of Immunology 149, no. 11 (1992): 3605–11. http://dx.doi.org/10.4049/jimmunol.149.11.3605.

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Abstract The maternally transmitted Ag is a cell surface product of three gene products: 1) H-2M3a (formerly Hmta), a class I MHC heavy chain; 2) beta 2-microglobulin; and 3) maternally transmitted factor (Mtf), the N-terminus of the mitochondrially encoded ND1 subunit of the reduced form of nicotinamide-adenine dinucleotide dehydrogenase. This class I molecule has been shown to be an N-formyl peptide receptor. Although the N-formyl moiety is necessary for binding to M3a, it is not sufficient. We proposed that the R group of the amino acid in position 1 plays a pivotal role in peptide binding
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36

Lin, Zhi-Dong, and Wen Zeng. "Aquabis(2-formyl-6-methoxyphenolato)copper(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 5 (2006): m1074—m1076. http://dx.doi.org/10.1107/s1600536806013559.

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In the title mononuclear complex, [Cu(C8H7O3)2(H2O)], the CuII atom is five-coordinated by four O atoms from two 2-formyl-6-methoxyphenolate ligands and one O atom from a water molecule, to form a slightly distorted square-pyramidal coordination geometry. Centrosymmetric dimers are formed through intermolecular O—H...O hydrogen bonds, and these dimers are further linked by weak C—H...O hydrogen bonds to form a three-dimensional network.
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37

Zhang, Hong-Hai. "Diaquabis(4-formyl-2-methoxyphenolato)iron(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): m3325—m3327. http://dx.doi.org/10.1107/s1600536806047064.

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38

Collas, Alain, Christophe M. L. Vande Velde, and Frank Blockhuys. "2-(4-Formyl-2,6-dimethoxyphenoxy)acetic acid." Acta Crystallographica Section E Structure Reports Online 66, no. 11 (2010): o3003. http://dx.doi.org/10.1107/s1600536810043990.

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39

Chen, Xin, and Ming Yu. "4-Bromo-2-formyl-6-methoxyphenyl benzenesulfonate." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o646—o647. http://dx.doi.org/10.1107/s1600536807000517.

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40

Daoubi, M., and A. Benharref. "2-Formyl nor-31-lanosten-3-enol." Molecules 6, no. 6 (2001): M223. http://dx.doi.org/10.3390/m223.

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41

Gao, Shan, Li-Hua Huo, Xian-Fa Zhang, and Hui Zhao. "Triaquaformatobis(4-formyl-2-methoxyphenolato)gadolinium(III)." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (2004): m1738—m1740. http://dx.doi.org/10.1107/s1600536804027205.

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42

Sadaoka, Kana, Toru Oba, Hitoshi Tamiaki, Shigenori Kashimura, and Yoshitaka Saga. "Demetalation kinetics of the zinc chlorophyll derivative possessing two formyl groups: effects of formyl groups conjugated to the chlorin macrocycle on physicochemical properties of photosynthetic pigments." Journal of Porphyrins and Phthalocyanines 17, no. 11 (2013): 1120–28. http://dx.doi.org/10.1142/s1088424613500788.

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Demetalation kinetics of zinc chlorophyll derivative 1 possessing two formyl groups directly linked to the A- and B-rings of the chlorin macrocycle, which was synthesized from chlorophyll b, was examined under acidic conditions and compared with those of Zn chlorins 2 and 3 possessing a single formyl group in the A- and B-ring, respectively, as well as Zn chlorin 4 lacking any formyl group to unravel the substitution effects on demetalation properties of chlorophyllous pigments. Demetalation kinetics of diformylated Zn chlorin 1 was slower than those of monoformylated Zn chlorins 2 and 3, indi
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43

Qi, Ai-Di, Qing-Hua Zhu, Yong-Zhi He, and Xiao-Liang Ren. "4-{2-[2-(4-Formyl-2-methoxyphenoxy)ethoxy]ethoxy}-3-methoxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3784—o3785. http://dx.doi.org/10.1107/s1600536805033283.

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44

Dong, Yan. "(4-Formyl-2-methoxyphenolato)tris(2-methyl-2-phenylpropyl)tin(IV)." Acta Crystallographica Section E Structure Reports Online 64, no. 3 (2008): m450. http://dx.doi.org/10.1107/s1600536808003437.

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45

N., Venkatesh Kumar, Suhramani B., and P. Rajendran S. "A new synthesis of 5-substituted-3-phenyl-2H-pyrano[2,3-b ]quinolin-2-ones." Journal of Indian Chemical Society Vol. 80, Oct 2003 (2003): 918–20. https://doi.org/10.5281/zenodo.5839422.

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Department of Chemistry. Bharathiar University, Coimbatore-641 046, India <em>Manuscript received 17 May 2002, accepted 23 May 2003</em> Synthesis of title compounds and derivatives is reported by the Perkin reaction of 3-formyl-4-phenyl/methyl-2-quinolones (3) with sodium salt of phenylacetic acid. The 3-formyl-2-quinolones 3 were obtained from 2-chloro-3-forml-4-phenyl/ methylquinolines (2) which ilium were prepared from 2-chloro-4-phenyl/methyl-3-vinylquinolines (1).
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46

Kim, Min Joon, Sophie M. Gaube, Michael H. R. Beh, Craig D. Smith, and Alison Thompson. "Synthesis and reactivity of 2-thionoester pyrroles: a route to 2-formyl pyrroles." RSC Advances 9, no. 54 (2019): 31773–80. http://dx.doi.org/10.1039/c9ra07527e.

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47

Miranda-Sánchez, Diter, Carlos H. Escalante, Dulce Andrade-Pavón, et al. "Pyrrole-Based Enaminones as Building Blocks for the Synthesis of Indolizines and Pyrrolo[1,2-a]pyrazines Showing Potent Antifungal Activity." Molecules 28, no. 20 (2023): 7223. http://dx.doi.org/10.3390/molecules28207223.

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Abstract:
As a new approach, pyrrolo[1,2-a]pyrazines were synthesized through the cyclization of 2-formylpyrrole-based enaminones in the presence of ammonium acetate. The enaminones were prepared with a straightforward method, reacting the corresponding alkyl 2-(2-formyl-1H-pyrrol-1-yl)acetates, 2-(2-formyl-1H-pyrrol-1-yl)acetonitrile, and 2-(2-formyl-1H-pyrrol-1-yl)acetophenones with DMFDMA. Analogous enaminones elaborated from alkyl (E)-3-(1H-pyrrol-2-yl)acrylates were treated with a Lewis acid to afford indolizines. The antifungal activity of the series of substituted pyrroles, pyrrole-based enaminon
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48

Kawahara, Kan, Masayoshi Matsumoto, Harukichi Hashimoto, and Sotaro Miyano. "Kinetic Resolution of 2-Formyl-1,1′-binaphthyls by Baker’s-Yeast Reduction of the Formyl Function." Chemistry Letters 17, no. 7 (1988): 1163–64. http://dx.doi.org/10.1246/cl.1988.1163.

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49

Lü, Qiang, Xinting Lu, Jisheng Zhang, et al. "Synthesis and Bioactivity of 2-(Pyridyl-2-formyl)pyrimidine Derivatives." Chinese Journal of Organic Chemistry 35, no. 6 (2015): 1342. http://dx.doi.org/10.6023/cjoc201412034.

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50

Meyer, Walter L., Michael J. Brannon, Andrew Merritt, and Dieter Seebach. "Annulation of 2-formyl-2-cyclohexenones by reaction with enamines." Tetrahedron Letters 27, no. 13 (1986): 1449–52. http://dx.doi.org/10.1016/s0040-4039(00)84282-3.

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