Relevant bibliographies by topics / Indole-3-carboxylic acids

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Academic literature on the topic 'Indole-3-carboxylic acids'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Indole-3-carboxylic acids"

1

Lynch, Daniel E., Tariq Latif, Graham Smith, Karl A. Byriel, Colin H. L. Kennard, and Simon Parsons. "Molecular Cocrystals of Carboxylic Acids. XXXI Adducts of 2-Aminopyrimidine and 3-Amino-1,2,4-triazole with Heterocyclic Carboxylic Acids." Australian Journal of Chemistry 51, no. 5 (1998): 403. http://dx.doi.org/10.1071/c97201.

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A series of molecular adducts of 2-aminopyrimidine and 3-amino-1,2,4-triazole with heterocyclic carboxylic acids have been prepared and characterized by using X-ray powder diffraction and in four cases by single-crystal X-ray diffraction methods. These four compounds are the (1 : 1) adducts of 2-aminopyrimidine with indole-3-acetic acid [(C4H5N3)(C10H9NO2)], N-methylpyrrole-2-carboxylic acid [(C4H5N3)(C6H7NO2)] and thiophen-2-carboxylic acid [(C4H5N3)(C5H4O2S)], and the (1 : 1) adduct of 3-amino-1,2,4-triazole with thiophen-2-carboxylic acid [(C2H4N4)(C5H4O2S)]. Other compounds described are t
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2

Buttery, Cheryl D., Richard G. Jones, and David W. Knight. "Homologation of Indole-3-carboxylic Acids and Amides." Synlett 1991, no. 04 (1991): 315–16. http://dx.doi.org/10.1055/s-1991-20713.

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3

Buttery, Cheryl D., Richard G. Jones, and David W. Knight. "Homologation of Indole-3-carboxylic Acids and Amides." Synlett 1991, no. 05 (1991): 315–16. http://dx.doi.org/10.1055/s-1991-34725.

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4

Kim, Youseung, Ho Joon Song, Min Yi Kim, Soon Bang Kang, and Bong Young Chung. "Synthesis of Indole-fused 4-Pyridone-3-carboxylic Acids." HETEROCYCLES 48, no. 1 (1998): 103. http://dx.doi.org/10.3987/com-97-8018.

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5

Laronze, Marie, Jean-Yves Laronze, Csaba Nemes, and Janos Sapi. "Oxidative Transformation of Indole-3-acetonitrile Derivatives into the Corresponding Indole-3-carboxylic Acids." European Journal of Organic Chemistry 1999, no. 9 (1999): 2285–91. http://dx.doi.org/10.1002/(sici)1099-0690(199909)1999:9<2285::aid-ejoc2285>3.0.co;2-n.

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6

Shao, Zhuzhou, Lubin Xu, Liang Wang, Hongtao Wei, and Jian Xiao. "Catalyst-free tandem Michael addition/decarboxylation of (thio)coumarin-3-carboxylic acids with indoles: facile synthesis of indole-3-substituted 3,4-dihydro(thio)coumarins." Org. Biomol. Chem. 12, no. 14 (2014): 2185–88. http://dx.doi.org/10.1039/c3ob42582g.

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The tandem Michael addition/decarboxylation of (thio)-coumarin-3-carboxylic acids with indoles gives biologically important indole-3-substituted dihydrocoumarins in good to excellent yields under catalyst-free conditions.
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7

Silvestri, R., M. Artico, B. Bruno, et al. "Synthesis and Biological Evaluation of 5H-Indolo [3,2-b][1,5]Benzothiazepine Derivatives, Designed as Conformationally Constrained Analogues of the Human Immunodeficiency Virus Type 1 Reverse Transcriptase Inhibitor L-737,126." Antiviral Chemistry and Chemotherapy 9, no. 2 (1998): 139–48. http://dx.doi.org/10.1177/095632029800900205.

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In the presence of sodium hydride, reaction of aryldisulphides with ethyl esters of indole-2-carboxylic acids furnished ethyl 3-arylthioindole-2-carboxy-lates, which were cyclized intramolecularly to afford 5 H-indolo[3,2-b][1,5]benzothiazepin-6(7 H)-ones or hydrolysed in alkaline medium to give 3-arylthioindole-2-carboxylic acids. These acids, also obtained by the action of aryldisulphides on indole-2-carboxylic acids, afforded tetracyclic 5 H-indolo [3,2-b][1,5]benzothiazepin-6(7 H)-ones upon treatment with EDCI–DMAP. Transformation of cyclic sulphides into the required sulphones was achieve
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8

Piu, Paola, Vittorio Leoni, M. Antonietta Zoroddu, Gavina Manca, Salvatore Deiana та Carlo Gessa. "Coordination of metal ions by indolic acids. Complexes of indole-3-carboxylic, indole-3-acetic, indole-3-β-acrylic, indole-N-acetic and indole-N-methyl-2-carboxylic acids with some divalent metal ions". Transition Metal Chemistry 17, № 4 (1992): 283–86. http://dx.doi.org/10.1007/bf02910889.

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9

Lynch,, Daniel E., Graham Smith, Karl A. Byriel,, Colin H. L. Kennard,, Johann Kwiatkowski, and Andrew K. Whittaker. "Molecular Cocrystals of Carboxylic Acids. XXVII An Investigation into the Use of Triphenylphosphine Oxide Cocrystals for Non-Linear Optics: the Crystal Structure of the Adduct of Triphenylphosphine Oxide with N-Methylpyrrole-2-carboxylic Acid." Australian Journal of Chemistry 50, no. 12 (1997): 1191. http://dx.doi.org/10.1071/c97113.

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Four adducts of triphenylphosphine oxide with aromatic carboxylic acids have been synthesized and tested for second-order non-linear optical properties. These were with N-methylpyrrole-2-carboxylic acid (1), indole-2-carboxylic acid (2), 3-dimethylaminobenzoic acid (3), and thiophen-2-carboxylic acid (4). Compound (1) produced clear, colourless crystals (space group P 212121 with a 9·892(1), b 14·033(1), c 15·305(1) Å, Z 4) which allowed the structure to be determined by X-ray diffraction.
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10

Purwono, Bambang, Naresh Kumar, and David StC Black. "Approaches to calix[3]indoles from activated indole carboxylic acids." Arkivoc 2022, no. 4 (2021): 6–23. http://dx.doi.org/10.24820/ark.5550190.p011.637.

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Book chapters on the topic "Indole-3-carboxylic acids"

1

Taber, Douglass F. "Heteroaromatics: The Mal Synthesis of Clausevatine D." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0066.

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Huanfeng Jiang of the South China University of Technology showed (J. Org. Chem. 2010, 75, 966) that an alkynoate 1 could be condensed with a 1,3-dicarbonyl compound 2 to give, under oxidizing conditions, the furan 3. Phil Ho Lee of Kangwon National University found (Tetrahedron Lett. 2010, 51, 1899) that the enyne 4 cyclized smoothly to the furan 5. Yahong Li of Suzhou University and Vladimir Gevorgyan of the University of Illinois, Chicago, demonstrated (J. Am. Chem. Soc. 2010, 132, 7645) that the cyclization of 6 proceeded with silyl migration, to give 7. François Bilodeau and Pat Forgione
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Taber, Douglass F. "Best Synthetic Methods: Oxidation." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0009.

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Karl A. Scheidt of Northwestern University described (Organic Lett. 2009, 11, 1651) the oxidation of primary alcohols such as 1 in the presence of an indole 2. The product 3, an active acylating agent, is readily converted to other esters and amides. K. Rajender Reddy of the Indian Institute of Chemical Technology, Hyderabad, developed (Tetrahedron Lett. 2009, 50, 2050) a protocol for the direct oxidation of a primary amine 4 to the corresponding nitrile 5. In the presence of ammonia, the same procedure converted aldehydes and primary alcohols into the nitriles. Several catalytic methods for t
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