Relevant bibliographies by topics / 3H-indoles

Academic literature on the topic '3H-indoles'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "3H-indoles"

1

Le Count, David J., and Anthony P. Marson. "Cycloadditions of 3H-indoles." Journal of the Chemical Society, Perkin Transactions 1, no. 3 (1988): 451. http://dx.doi.org/10.1039/p19880000451.

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2

Zhu, Jiawei, Song Sun, Minfang Xia, Ning Gu, and Jiang Cheng. "Copper-catalyzed radical 1,2-cyclization of indoles with arylsulfonyl hydrazides: access to 2-thiolated 3H-pyrrolo[1,2-a]indoles." Organic Chemistry Frontiers 4, no. 11 (2017): 2153–55. http://dx.doi.org/10.1039/c7qo00478h.

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3

Archana. "SYNTHESIS AND EVALUATION OF SOME NEWER QUINAZOLINONYL SUBSTITUTED BENZOXAZEPINYL / BENZOTHIAZEPINYL INDOLES AS POTENT ANTICONVULSANT AGENTS." INDIAN DRUGS 56, no. 03 (March 28, 2019): 18–24. http://dx.doi.org/10.53879/id.56.03.11538.

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new series of 3-[3-amino-2-methyl-6-substituted quinazolin-4(3H)-onyl chalconyl)-2-substituted indoles (3-8), 3-[3-Amino-2-methyl-6- substituted quinazolin-4(3H) -onyl-benzoxazepin/benzo -thiazepin- 2-yl] -2-substituted indoles (9-20) and 3-[3-amino-2-methyl-6-substituted quinazolin-4(3H) -onyl-3- (sub-stituted phenylaminomethylene) -benzoxazepin/benzothizepin-2-yl] -2-substitutedindoles (21-44) were synthesised and evaluated for anticonvulsant activity. All these compounds were screened in vivo, for their anticonvulsant activity and acute toxicity. Coumpund 44 , 3-[3-amino-2-methyl-6-bromoquinazolin- 4(3H)-onyl-3- (chlorophenylaminomethylene)-benzothiazepine-2-yl]-2-chloroindole, was found to be most potent compound of this series , more potent than standard drug phenytoin sodium. The homogeneity of all the compounds have been established by elemental analysis, IR and 1H-NMR spectroscopy.
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4

Zhou, Qianting, Xia Song, Xinying Zhang, and Xuesen Fan. "Synthesis of 3-spirooxindole 3H-indoles through Rh(iii)-catalyzed [4 + 1] redox-neutral spirocyclization of N-aryl amidines with diazo oxindoles." Organic Chemistry Frontiers 8, no. 15 (2021): 4131–37. http://dx.doi.org/10.1039/d1qo00551k.

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5

Grishin, Igor Yu, Nikolai A. Arutiunov, Dmitrii A. Aksenov, Nicolai A. Aksenov, Alexander V. Aksenov, Amina Z. Gasanova, Elena A. Sorokina, Carolyn Lower, and Michael Rubin. "Improved Method for Preparation of 3-(1H-Indol-3-yl)benzofuran-2(3H)-ones." Molecules 27, no. 6 (March 15, 2022): 1902. http://dx.doi.org/10.3390/molecules27061902.

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6

Trofimov, Boris, Ludmila Oparina, Nikita Kolyvanov, Igor Ushakov, Anastasiya Mal’kina, and Alexander Vashchenko. "Metal- and Solvent-free Synthesis of Functionalized Dihydrooxa­zolo[3,2-a]indoles by One-Pot Tandem Assembly of 3H-Indoles and Propargylic Alcohols." Synthesis 51, no. 06 (November 28, 2018): 1445–54. http://dx.doi.org/10.1055/s-0037-1610319.

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The reaction of 3H-indoles with tertiary propargylic alcohols to give functionalized dihydrooxazolo[3,2-a]indoles in good to excellent yields has been developed. This metal- and solvent-free, one-pot tandem assembly proceeds under mild conditions (22–60 °C) and is regio- and stereoselective: either the Z- or E-isomers (relative to the double bond) are alternatively formed depending on other functionalized substituents on the propargylic alcohols.
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7

López, Concepción, Asensio González, Carlos Moya, Ramon Bosque, Xavier Solans, and Mercè Font-Bardía. "Cyclopalladation of 3-methoxyimino-2-phenyl-3H-indoles." Journal of Organometallic Chemistry 693, no. 17 (August 2008): 2877–86. http://dx.doi.org/10.1016/j.jorganchem.2008.05.043.

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8

Yavari, Issa, Mehdi Adib, and Mohammad H. Sayahi. "Efficient synthesis of functionalized 3H-pyrrolo[1,2-a]indoles." Journal of the Chemical Society, Perkin Transactions 1, no. 13 (June 10, 2002): 1517–19. http://dx.doi.org/10.1039/b204433c.

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9

González, Asensio, and Carmen Gálvez. "Preparation of 2-Acylaminobenzonitriles from 3-Hydroxyimino-3H-indoles." Synthesis 1982, no. 11 (May 15, 2002): 946. http://dx.doi.org/10.1055/s-1982-30011.

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10

Giordani, Cristiana, Emanuela Licandro, Stefano Maiorana, Antonio Papagni, Alexandra M. Slawin, and David J. William. "Reactions of chromium (methoxymethyl)carbene complexes with 3H-indoles." Journal of Organometallic Chemistry 393, no. 2 (August 1990): 227–36. http://dx.doi.org/10.1016/0022-328x(90)80202-b.

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Dissertations / Theses on the topic "3H-indoles"

1

單慧媚 and Wai-mei Della Sin. "Addition reactions of 3H-indoles and their N-oxides." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1992. http://hub.hku.hk/bib/B31233193.

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