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Journal articles on the topic '3H-indoles'

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Published: 10 December 2022
Last updated: 28 January 2023

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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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11

Martins, Guilherme M., Gilson Zeni, Davi F. Back, Teodoro S. Kaufman, and Claudio C. Silveira. "Expedient Iodocyclization Approach Toward Polysubstituted 3H-Benzo[e]indoles." Advanced Synthesis & Catalysis 357, no. 14-15 (September 28, 2015): 3255–61. http://dx.doi.org/10.1002/adsc.201500275.

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12

KATAYAMA, Sadamu, Toshio WATANABE, and Masashige YAMAUCHI. "Convenient Synthesis of 3H-Indoles(Indolenines) by Reaction of 1H-Indoles with Corey-Kim Reagent." CHEMICAL & PHARMACEUTICAL BULLETIN 40, no. 10 (1992): 2836–38. http://dx.doi.org/10.1248/cpb.40.2836.

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13

Arcadi, Antonio, Emanuela Pietropaolo, Antonello Alvino, and Véronique Michelet. "Aminofluorination of 2-alkynylanilines: a Au-catalyzed entry to fluorinated indoles." Beilstein Journal of Organic Chemistry 10 (February 20, 2014): 449–58. http://dx.doi.org/10.3762/bjoc.10.42.

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The scope and limitations of gold-catalyzed tandem cycloisomerization/fluorination reactions of unprotected 2-alkynylanilines to have access to 3,3-difluoro-2-aryl-3H-indoles and 3-fluoro-2-arylindoles are described. An unprecedented aminoauration/oxidation/fluorination cascade reaction of 2-alkynylanilines bearing a linear alkyl group on the terminal triple bond is reported.
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14

Rueping, Magnus, Teerawut Bootwicha, and Erli Sugiono. "Continuous-flow catalytic asymmetric hydrogenations: Reaction optimization using FTIR inline analysis." Beilstein Journal of Organic Chemistry 8 (February 23, 2012): 300–307. http://dx.doi.org/10.3762/bjoc.8.32.

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The asymmetric organocatalytic hydrogenation of benzoxazines, quinolines, quinoxalines and 3H-indoles in continuous-flow microreactors has been developed. Reaction monitoring was achieved by using an inline ReactIR flow cell, which allows fast and convenient optimization of reaction parameters. The reductions proceeded well, and the desired products were isolated in high yields and with excellent enantioselectivities.
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15

Rodríguez, J. G., Y. Benito, and F. Temprano. "Synthesis of spiro[cycloalkane-1,3′-[3H]indoles] from cycloalkanecarbaldehydes. Acid-catalyzed rearrangement to cycloalkano[b]indoles." Journal of Heterocyclic Chemistry 22, no. 5 (September 1985): 1207–10. http://dx.doi.org/10.1002/jhet.5570220512.

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16

Li, Z., Z. He, and H. Li. "Intramolecular Cyclization of Enamines to 3H-Indoles Mediated by Iodine." Synfacts 2010, no. 09 (August 23, 2010): 0987. http://dx.doi.org/10.1055/s-0030-1258000.

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17

Desarbre, E., L. Savelon, O. Cornec, and J. Y. Mérour. "Oxidation of indoles and 1,2-dihydro-3H-indol-3-ones." Tetrahedron 52, no. 8 (February 1996): 2983–94. http://dx.doi.org/10.1016/0040-4020(96)00001-4.

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18

KATAYAMA, S., T. WATANABE, and M. YAMAUCHI. "ChemInform Abstract: Convenient Synthesis of 3H-Indoles (Indolenines) by Reaction of 1H- Indoles with Corey-Kim Reagent." ChemInform 24, no. 42 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199342166.

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19

He, Zhiheng, Huanrong Li, and Zhiping Li. "Iodine-Mediated Synthesis of 3H-Indoles via Intramolecular Cyclization of Enamines." Journal of Organic Chemistry 75, no. 13 (July 2, 2010): 4636–39. http://dx.doi.org/10.1021/jo100796s.

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20

Kagawa, Natsuko, Hiroki Takabatake, and Yoshitake Masuda. "Synthesis of 3′-allylindoline spirobenzopyrans derived from 3-allyl-3H-indoles." Tetrahedron Letters 55, no. 47 (November 2014): 6427–31. http://dx.doi.org/10.1016/j.tetlet.2014.09.121.

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21

Chetverikov, V. P., G. A. Titov, Yu G. Bundel', M. S. Luk'yanova, and V. M. Kurilenko. "Synthesis and pharmacological activity of 3H-[1,4]diazepino-[2,3-g]indoles." Pharmaceutical Chemistry Journal 21, no. 12 (December 1987): 874–78. http://dx.doi.org/10.1007/bf00757965.

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22

Rueping, Magnus, Claus Brinkmann, Andrey P. Antonchick, and Iuliana Atodiresei. "Asymmetric Synthesis of Indolines by Catalytic Enantioselective Reduction of 3H-Indoles." Organic Letters 12, no. 20 (October 15, 2010): 4604–7. http://dx.doi.org/10.1021/ol1019234.

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23

Martins, Guilherme M., Gilson Zeni, Davi F. Back, Teodoro S. Kaufman, and Claudio C. Silveira. "ChemInform Abstract: Expedient Iodocyclization Approach Toward Polysubstituted 3H-Benzo[e]indoles." ChemInform 47, no. 9 (February 2016): no. http://dx.doi.org/10.1002/chin.201609148.

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24

Capdevielle, Patrice, and Michel Maumy. "Copper-catalyzed oxidation of indoles by dioxygen. Synthesis of 2-aryl and 2-amino 3-oxo 3H-indoles." Journal of Inorganic Biochemistry 47, no. 3-4 (July 1992): 47. http://dx.doi.org/10.1016/0162-0134(92)84119-8.

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25

Karrick, Gregory L., and Norton P. Peet. "A reinvestigation of the synthesis of 3H-[1,2]diazepino[5,6-b]indoles. The synthesis of pyrido[4,3-b]indoles." Journal of Heterocyclic Chemistry 23, no. 4 (July 1986): 1055–57. http://dx.doi.org/10.1002/jhet.5570230418.

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26

DESARBRE, E., L. SAVELON, O. CORNEC, and J. Y. MEROUR. "ChemInform Abstract: Oxidation of Indoles and 1,2-Dihydro-3H-indol-3-ones." ChemInform 27, no. 25 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199625117.

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27

Kong, Chen, and Tom G. Driver. "Rh2(II)-Catalyzed Ester Migration to Afford 3H-Indoles from Trisubstituted Styryl Azides." Organic Letters 17, no. 4 (February 2, 2015): 802–5. http://dx.doi.org/10.1021/ol503541z.

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28

Rueping, Magnus, Claus Brinkmann, Andrey P. Antonchick, and Iuliana Atodiresei. "ChemInform Abstract: Asymmetric Synthesis of Indolines by Catalytic Enantioselective Reduction of 3H-Indoles." ChemInform 42, no. 7 (January 20, 2011): no. http://dx.doi.org/10.1002/chin.201107148.

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29

Rodante, F., G. Marrosu, and G. Catalani. "Thermal analysis of 2-phenyl-3-arylimino-3H-indoles using simultaneous TG-DSC." Thermochimica Acta 185, no. 2 (August 1991): 303–14. http://dx.doi.org/10.1016/0040-6031(91)80052-k.

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30

Bastide, Jean, Philippe Carre, Francis Gomez, and Alfred Greiner. "Metabolism of phenyl-3H-indoles by cell suspension ofAcer pseudoplatanusL. and their phytotoxicity." Pesticide Science 27, no. 1 (1989): 33–43. http://dx.doi.org/10.1002/ps.2780270105.

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31

He, Zhiheng, Huanrong Li, and Zhiping Li. "ChemInform Abstract: Iodine-Mediated Synthesis of 3H-Indoles via Intramolecular Cyclization of Enamines." ChemInform 41, no. 45 (October 14, 2010): no. http://dx.doi.org/10.1002/chin.201045111.

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32

Letcher, Roy M., Della W. M. Sin, and Kung-Kai Cheung. "Oxazolo[3,2-a]indoles, pyrrolo- and azepino-[1,2-a]indoles from 3H-indole 1-oxides and acetylenecarboxylic esters by skeletal rearrangements." Journal of the Chemical Society, Perkin Transactions 1, no. 8 (1993): 939. http://dx.doi.org/10.1039/p19930000939.

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33

Harada, Kazuho, Hitoshi Someya, and Shonosuke Zen. "New Heterocyclic Ring Systems: The Syntheses of 2H,3H,7H-Imidazo[1',2':1,2]pyrido[4,3-b]indoles and 2H,3H,4H,8H-Pyrimido[1',2':1,2]pyrido[4,3-b]indoles." HETEROCYCLES 38, no. 8 (1994): 1867. http://dx.doi.org/10.3987/com-94-6756.

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34

Capdevielle, Patrice, and Michel Maumy. "3-Oxo 3H-indole from dioxygen copper-catalyzed oxidation of indole: One-flask synthesis of 2-dialkylamino 3-oxo 3H-indoles." Tetrahedron Letters 34, no. 18 (April 1993): 2953–56. http://dx.doi.org/10.1016/s0040-4039(00)60490-2.

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35

Li, Yunyun, Zisong Qi, He Wang, Xifa Yang, and Xingwei Li. "Ruthenium(II)-Catalyzed C−H Activation of Imidamides and Divergent Couplings with Diazo Compounds: Substrate-Controlled Synthesis of Indoles and 3H-Indoles." Angewandte Chemie International Edition 55, no. 39 (August 25, 2016): 11877–81. http://dx.doi.org/10.1002/anie.201606316.

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36

Li, Yunyun, Zisong Qi, He Wang, Xifa Yang, and Xingwei Li. "Ruthenium(II)-Catalyzed C−H Activation of Imidamides and Divergent Couplings with Diazo Compounds: Substrate-Controlled Synthesis of Indoles and 3H-Indoles." Angewandte Chemie 128, no. 39 (August 25, 2016): 12056–60. http://dx.doi.org/10.1002/ange.201606316.

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37

Belletete, Michel, and Gilles Durocher. "Conformational changes upon excitation of dimethylamino para-substituted 3H-indoles: viscosity and solvent effects." Journal of Physical Chemistry 93, no. 5 (March 1989): 1793–99. http://dx.doi.org/10.1021/j100342a022.

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38

Ziegler, Frederick E., and Lucio O. Jeroncic. "A new route to 9,9a-Dihydro-3H-pyrrolo[1,2-a]indoles via radical cyclization." Journal of Organic Chemistry 56, no. 11 (May 1991): 3479–86. http://dx.doi.org/10.1021/jo00011a008.

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39

Baradarani, Mehdi M., Arash Afghan, Farideh Zebarjadi, Kamal Hasanzadeh, and John A. Joule. "The synthesis of 3,3-dimethyl-2-(1-aryl-1h-pyrazol-4-yl)-3h-indoles." Journal of Heterocyclic Chemistry 43, no. 6 (November 2006): 1591–95. http://dx.doi.org/10.1002/jhet.5570430624.

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40

Drouhin, Pauline, and Richard J. K. Taylor. "A Copper-Mediated Oxidative Coupling Route to 3H- and 1H-Indoles fromN-Aryl-enamines." European Journal of Organic Chemistry 2015, no. 11 (March 13, 2015): 2333–36. http://dx.doi.org/10.1002/ejoc.201500112.

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41

HARADA, K., H. SOMEYA, and S. ZEN. "ChemInform Abstract: New Heterocyclic Ring Systems: The Syntheses of 2H,3H,7H-Imidazo(1′2′: 1,2)pyrido(4,3.b)indoles and 2H,3H,4H,8H-Pyrimido(1′,2′:1,2)pyrido(4,3- b)indoles." ChemInform 25, no. 47 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199447169.

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42

Jones, Keith, and John M. D. Storey. "Intramolecular organolithium addition to indol-2(3H )-ones; an approach to the synthesis of pyrrolo[1,2-a]indoles and pyrido[1,2-a]indoles." Journal of the Chemical Society, Perkin Transactions 1, no. 5 (2000): 769–74. http://dx.doi.org/10.1039/a909548i.

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43

LETCHER, R. M., D. W. M. SIN, and K. K. CHEUNG. "ChemInform Abstract: Oxazolo(3,2-a)indoles, Pyrrolo- and Azepino-(1,2-a)indoles from 3H- Indole 1-Oxides and Acetylenecarboxylic Esters by Skeletal Rearrangements." ChemInform 24, no. 34 (September 1, 2010): no. http://dx.doi.org/10.1002/chin.199334163.

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44

El-Gendy, Adel A., and Jochen Lehmann. "Indoles, IV 9-Substituted 4,9-Dihydropyrano[3,4-b]indol-1(3H)-ones - Synthesis and Conversion into 2,3,4,9-Tetrahydro- 1H-pyrido-[3,4-b]indoles." Archiv der Pharmazie 320, no. 8 (1987): 698–704. http://dx.doi.org/10.1002/ardp.19873200806.

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45

W. G. Fishwick, Colin, Andrew D. Jones, and Michael B. Mitchell. "Regio- and Chemoselective Alkylation of 2,3-Dialkylindoles. A Convenient Preparation of 2,3,3-Trialkyl-3H-indoles." HETEROCYCLES 32, no. 4 (1991): 685. http://dx.doi.org/10.3987/com-90-5446.

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46

Hu, Haoxiang, Chunna Meng, Yun Dong, Xin Li, and Jinxing Ye. "Catalytic Asymmetric Formal Aza-Diels–Alder Reactions of α,β-Unsaturated Ketones and 3H-Indoles." ACS Catalysis 5, no. 6 (May 20, 2015): 3700–3703. http://dx.doi.org/10.1021/acscatal.5b00680.

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47

Sarpal, Ranjit S., Michel Belletête, and Gilles Durocher. "Temperature effects on the solubilization behavior of some 3H-indoles in water and microheterogeneous media." Journal of Photochemistry and Photobiology A: Chemistry 86, no. 1-3 (February 1995): 201–7. http://dx.doi.org/10.1016/1010-6030(94)03939-r.

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48

Dige, Nilam C., and Dattaprasad M. Pore. "Green Aspect for Multicomponent Synthesis of Spiro[4H-indeno[1,2-b]pyridine-4,3′-[3H]indoles]." Synthetic Communications 45, no. 21 (October 6, 2015): 2498–510. http://dx.doi.org/10.1080/00397911.2015.1092551.

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49

Nigam, Shalini, Ranjit S. Sarpal, Michel Belletête, and Gilles Durocher. "3H-Indoles in Cetyltrimethylammonium Bromide (CTAB) Micelles and Water: Spectroscopy and Photophysics at Various Temperatures." Journal of Colloid and Interface Science 177, no. 1 (January 1996): 143–49. http://dx.doi.org/10.1006/jcis.1996.0014.

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50

Kong, Chen, and Tom G. Driver. "ChemInform Abstract: Rh2(II)-Catalyzed Ester Migration to Afford 3H-Indoles from Trisubstituted Styryl Azides." ChemInform 46, no. 28 (June 25, 2015): no. http://dx.doi.org/10.1002/chin.201528147.

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