Log in

Relevant bibliographies by topics / Dihydroindolone / Journal articles

Journal articles on the topic 'Dihydroindolone'

To see the other types of publications on this topic, follow the link: Dihydroindolone.

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Dihydroindolone.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Shishkina, Svitlana V., Igor V. Ukrainets, and Lidiya A. Petrushova. "(R,S)-2′-Amino-6′-methyl-2,5′,5′-trioxo-6′H-spiro[indoline-3,4′-pyrano[3,2-c][2,1]benzothiazine]-3′-carbonitrile dimethylformamide monosolvate." Acta Crystallographica Section E Structure Reports Online 70, no. 7 (June 18, 2014): o786—o787. http://dx.doi.org/10.1107/s1600536814013634.

Full text

Abstract:

The title solvate, C20H14N4O4S·C3H7NO, comprises a stereogenic centre but the centrosymmetric space group causes the presence of the racemate in the crystal. The spiro-joined fragments are almost orthogonal, with a dihedral angle of 86.8 (2)° between the mean planes of the pyrane ring and the dihydroindolone ring system. The atoms of the indolinone bicycle are coplanar, with an r.m.s. deviation of 0.005 Å. In the crystal, pairs of N—H...O hydrogen bonds link the molecules into centrosymmetric dimers which are linked to the dimethylformamide solvent molecules by further N—H...O hydrogen bonds. N—H...N hydrogen bonds link neighbouring dimers into [010] chains.

APA, Harvard, Vancouver, ISO, and other styles

2

Adam, Mohamed Shaker S. "Catalytic activity of nickel(II), copper(II) and oxovanadium(II)-dihydroindolone complexes towards homogeneous oxidation reactions." Applied Organometallic Chemistry 32, no. 4 (January 11, 2018): e4234. http://dx.doi.org/10.1002/aoc.4234.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Ginzinger, Werner, Vladimir Arion, Gerald Giester, Markus Galanski, and Bernhard Keppler. "Synthesis and structural peculiarities of gallium Complexes with novel paullone derivatives." Open Chemistry 6, no. 3 (September 1, 2008): 340–46. http://dx.doi.org/10.2478/s11532-008-0048-x.

Full text

Abstract:

Abstract9-Bromo-7,12-dihydroindolo[3,2-d][1]benzazepin-6-ylhydrazine was reacted with 2-acetylpyridine to give a Schiff base as a potential tridentate ligand. The reaction of this ligand with gallium chloride afforded complexes of 1:1 and 2:1 stoichiometry. The results of X-ray diffraction studies of the ligand and both gallium complexes are reported and compared with the data for a related gallium complex with a Schiff base obtained from 9-bromo-7,12-dihydroindolo[3,2-d][1]benzazepin-6-ylhydrazine and 2-hydroxybenzaldehyde.

APA, Harvard, Vancouver, ISO, and other styles

4

Chen, Mintao, Wenqing Zang, Yin Wei, and Min Shi. "A highly efficient method for the construction of cyclopropane-containing dihydroindole derivatives from indolemethylenecyclopropanes with DIAD and DEAD." Organic & Biomolecular Chemistry 18, no. 2 (2020): 333–36. http://dx.doi.org/10.1039/c9ob02520k.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Hung, Tran Quang, Sören Hancker, Alexander Villinger, Stefan Lochbrunner, Tuan Thanh Dang, Aleksej Friedrich, Wolfgang Breitsprecher, and Peter Langer. "Novel synthesis of 5-methyl-5,10-dihydroindolo[3,2-b]indoles by Pd-catalyzed C–C and two-fold C–N coupling reactions." Organic & Biomolecular Chemistry 13, no. 2 (2015): 583–91. http://dx.doi.org/10.1039/c4ob01723d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Savych, Iryna, Tim Gläsel, Alexander Villinger, Vyacheslav Ya Sosnovskikh, Viktor O. Iaroshenko, and Peter Langer. "Synthesis of functionalized 2-salicyloylfurans, furo[3,2-b]chromen-9-ones and 2-benzoyl-8H-thieno[2,3-b]indoles by one-pot cyclizations of 3-halochromones with β-ketoamides and 1,3-dihydroindole-2-thiones." Organic & Biomolecular Chemistry 13, no. 3 (2015): 729–50. http://dx.doi.org/10.1039/c4ob01730g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Irgashev, Roman A., Nikita A. Kazin, Grigory A. Kim, Gennady L. Rusinov, and Valery N. Charushin. "A new synthetic approach to fused nine-ring systems of the indolo[3,2-b]carbazole family through double Pd-catalyzed intramolecular C–H arylation." RSC Advances 6, no. 74 (2016): 70106–16. http://dx.doi.org/10.1039/c6ra11796a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Niedźwiecka-Kornaś, Anna, Elżbieta Bojarska, Jarosław Kamiński, and Zygmunt Kazimierczuk. "Anodic Methoxylation of Isatin." Zeitschrift für Naturforschung B 53, no. 5-6 (June 1, 1998): 620–24. http://dx.doi.org/10.1515/znb-1998-5-619.

Full text

Abstract:

Abstract Anodic metoxylation of isatin was investigated. The product formed contained a unique 3a.7a-dihydroindole ring system. 3a,7a-Dihydro-(Z)-3a,7a-dimetoxyisatin was isolated and characterized with a variety of spectroscopic methods.

APA, Harvard, Vancouver, ISO, and other styles

9

Tian, Guojian, Shengyun Cai, Xin Li, Hans Ågren, Qiaochun Wang, Jinhai Huang, and Jianhua Su. "A new D–A–π–A type organic sensitizer based on substituted dihydroindolo [2,3-b] carbazole and DPP unit with a bulky branched alkyl chain for highly efficient DSCs." Journal of Materials Chemistry A 3, no. 7 (2015): 3777–84. http://dx.doi.org/10.1039/c4ta05162a.

Full text

Abstract:

Two new D–A–π–A type metal-free organic dyes based on a dihydroindolo[2,3-b]carbazole donor have been synthesized for DSCs. Both dyes exhibited broad IPCE spectra, good photo-stability and high performance.

APA, Harvard, Vancouver, ISO, and other styles

10

Raner, KD, and AD Ward. "Heterocyclic Syntheses Through Electrophilic Ring Closure Reactions of ortho-Allylaniline Systems." Australian Journal of Chemistry 44, no. 12 (1991): 1749. http://dx.doi.org/10.1071/ch9911749.

Full text

Abstract:

Amide derivatives of 2-allylanilines have been prepared by metallation of the amide derivatives of the corresponding 2-bromoanilines and subsequent reaction with an allylic halide. The electrophile -promoted cyclization of these compounds has been investigated. The free allylanilines readily undergo aminomercuration to form unstable mercury derivatives of tetrahydroquinolines but the corresponding amide derivatives do not cyclize. Instead, oxymercuration of the double bond occurs. The allylanilines react with iodine to yield 3-iodo-1,2,3,4-tetrahydroquinolines. The anion of 2,2,2-trifluoro-N-[4-hydroxymethyl-2-(3-methylbut-2-enyl)phenyl] acetamide reacts with iodine to give a 2,3-dihydroindole. These iodinated compounds can be further cyclized with base to form 7,7a-dihydro-1H-azirino[1,2-a] indoles. One of these aziridine systems was cleaved with hydrogen chloride to form a mixture of chlorinated tetrahydroquinoline and dihydroindole analogous to the iodo systems.

APA, Harvard, Vancouver, ISO, and other styles

11

Manna, Ranjan K., P. Jaisankar, and Venkatachalam S. Giri. "Synthesis of Indole Alkaloids and Alkaloidal Precursors: An Improved Synthesis of Flavopereirine." Journal of Chemical Research 23, no. 6 (June 1999): 350–51. http://dx.doi.org/10.1177/174751989902300603.

Full text

Abstract:

Synthesis of flavopereirine 1, formal synthesis of isogeissoschizines 8 and dihydrocorynantheols 9 through the intermediacy of 3-(2-hydroxyethyl)-6,7-dihydroindolo[2,3-a]quinolizine 3 and also the unexpected formation of the β-carbolines 12 and 13 on Huang-Minion reaction of 2 are described.

APA, Harvard, Vancouver, ISO, and other styles

12

Zhao, Fei, Lei Zhang, Hailong Liu, Shengbin Zhou, and Hong Liu. "Microwave-assisted synthesis of 5,6-dihydroindolo[1,2-a]quinoxaline derivatives through copper-catalyzed intramolecular N-arylation." Beilstein Journal of Organic Chemistry 9 (November 14, 2013): 2463–69. http://dx.doi.org/10.3762/bjoc.9.285.

Full text

Abstract:

An efficient and practical protocol has been developed to synthesize 5,6-dihydroindolo[1,2-a]quinoxaline derivatives by CuI-catalyzed intramolecular N-arylation under microwave irradiation. This method rapidly afforded the tetracyclic products with good to excellent yields (83–97%) in short reaction times (45–60 min).

APA, Harvard, Vancouver, ISO, and other styles

13

Rayni, Ibtissam, Youness El Bakri, Chin-Hung Lai, Jihad Sebhaoui, El Mokhtar Essassi, and Joel T. Mague. "Crystal structure, DFT study and Hirshfeld surface analysis of 1-nonyl-2,3-dihydro-1H-indole-2,3-dione." Acta Crystallographica Section E Crystallographic Communications 75, no. 8 (July 12, 2019): 1140–44. http://dx.doi.org/10.1107/s2056989019009691.

Full text

Abstract:

In the title molecule, C17H23NO2, the dihydroindole portion is planar (r.m.s. deviation = 0.0157 Å) and the nonyl substituent is in an `extended' conformation. In the crystal, the nonyl chains intercalate and the dihydroindoledione units are associated through C—H...O hydrogen bonds to form micellar blocks. Based on the Hirshfeld surface analysis, the most important intermolecular interaction is the H...H interaction.

APA, Harvard, Vancouver, ISO, and other styles

14

Suchentrunk, Christof, and Nikolaus Korber. "Reduktion von Isochinolin und Indol mit Cäsium in flüssigem Ammoniak / Reduction of Isoquinoline and Indole with Cesium in Liquid Ammonia." Zeitschrift für Naturforschung B 58, no. 10 (October 1, 2003): 990–96. http://dx.doi.org/10.1515/znb-2003-1009.

Full text

Abstract:

Isoquinoline and indole were reduced with solutions of cesium in liquid ammonia and the resulting crystalline compounds isolated as ammonia-rich solvate crystals. The reduction of isoquinoline yields the anion bisisoquinoline-2,2’-diide in the compound Cs2C18H14N2 · (7/2) NH3 as the result of a coupling reaction. Indole is reduced to the 5,8-dihydroindolide anion in the ammoniate CsC8H8N · 3NH3. Both anions display interactions between their aromatic π-systems and the cesium cations.

APA, Harvard, Vancouver, ISO, and other styles

15

M屍our, Jean-Yves, and Laurence Savelon. "Fischer Reaction of 1-Acetyl-3-oxo-2,3-dihydroindole and 1-(p-Toluenesulfonyloxy)-3-oxo-2,3-dihydroindole." HETEROCYCLES 32, no. 5 (1991): 849. http://dx.doi.org/10.3987/com-91-5681.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Tang, Xiang-Ying, Yue-fa Gong, and Heng-rui Huo. "Metal-Free Synthesis of Pyrrolo[1,2-a]quinoxalines Mediated by TEMPO Oxoammonium Salts." Synthesis 50, no. 14 (June 13, 2018): 2727–40. http://dx.doi.org/10.1055/s-0037-1610131.

Full text

Abstract:

We herein describe a novel TEMPO oxoammonium salt initiated Pictet–Spengler reaction of imines, generated in situ from carbonyl compounds and pyrrole- or indole-containing substrates, to afford 4,5-dihydropyrrolo[1,2-a]quinoxalines or 5,6-dihydroindolo[1,2-a]quinoxalines in good to excellent yields. Moreover, a one-pot synthesis of a biologically important quinoxaline is achieved via a cyclization–dehydrogenation process using one equivalent of the oxoammonium salt.

APA, Harvard, Vancouver, ISO, and other styles

17

Beemelmanns, Christine, and Hans-Ulrich Reissig. "New samarium diiodide-induced cyclizations." Pure and Applied Chemistry 83, no. 3 (January 18, 2011): 507–18. http://dx.doi.org/10.1351/pac-con-10-09-06.

Full text

Abstract:

Samarium diiodide (SmI2) smoothly promotes the cyclizations of suitably substituted carbonyl compounds with styrene subunits leading to benzannulated cyclooctenes. The intramolecular samarium ketyl addition to arene or hetarene moieties enables a new, efficient, and highly stereoselective entry to dearomatized products such as hexahydronaphthalenes, steroid-like tetra- or pentacyclic compounds, or dihydroindole derivatives. The usefulness of the developed SmI2-induced cyclization method was demonstrated by the shortest formal total synthesis of the alkaloid strychnine.

APA, Harvard, Vancouver, ISO, and other styles

18

MEROUR, J. Y., and L. SAVELON. "ChemInform Abstract: Fischer Reaction of 1-Acetyl-3-oxo-2,3-dihydroindole and 1-(p- Toluenesulfonyloxy)-3-oxo-2,3-dihydroindole." ChemInform 22, no. 45 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199145152.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Kiu Lee, Chang, Kyu Ok Jeon, and Ji Sook Yu. "Tautomerization of 3a,7a-Dihydroindole-2,3,3a,4-tetracarboxylate." HETEROCYCLES 65, no. 8 (2005): 1989. http://dx.doi.org/10.3987/com-05-10457.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Lee, Do-Hun. "Rearrangement and Degradation of 3a,7a-Dihydroindole Esters." Asian Journal of Chemistry 28, no. 1 (2016): 185–88. http://dx.doi.org/10.14233/ajchem.2016.19317.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Zhang, Lei, Fei Zhao, Mingyue Zheng, Yun Zhai, Jiang Wang, and Hong Liu. "Selective Synthesis of 5,6-Dihydroindolo[1,2-a]quinoxalines and 6,7-Dihydroindolo[2,3-c]quinolines by Orthogonal Copper and Palladium Catalysis." European Journal of Organic Chemistry 2013, no. 25 (July 19, 2013): 5710–15. http://dx.doi.org/10.1002/ejoc.201300667.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Raner, KD, BW Skelton, AD Ward, and AH White. "Reactions of Epoxides Derived From 2′-(3″-Methylbut-2″-enyl)trifluoroacetanilides." Australian Journal of Chemistry 43, no. 3 (1990): 609. http://dx.doi.org/10.1071/ch9900609.

Full text

Abstract:

The intramolecular nucleophilic ring opening of the epoxides derived from 2′-(3″-methylbut-2″-enyl) trifluoroacetanilides has been investigated under both acidic and basic conditions. Boron trifluoride caused rearrangement of the epoxides to a ketone but no cyclization. Potassium carbonate in methanol caused regiospecific opening of the epoxides and generated dihydroindole products. The formation of a five-membered ring was confirmed by a single-crystal X-ray study of one of the products. The epoxides hydrolysed very readily in acidic conditions; the structure of one of the diol products was confirmed by a single-crystal X-ray study.

APA, Harvard, Vancouver, ISO, and other styles

23

Yogavel, M., D. Velmurugan, W. G. Rajeswaran, P. C. Srinivasan, and H. K. Fun. "1,2,3-Trimethoxy-5,11-dihydroindolo[1,2-b]isoquinoline-5,11-dione." Acta Crystallographica Section C Crystal Structure Communications 61, no. 12 (November 19, 2005): o715—o717. http://dx.doi.org/10.1107/s0108270105035158.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Braekman, J. C., C. Hootele, C. van Moorleghem, M. Kaisin, J. Pecher, L. D. Antonaccio, and B. Gilbert. "Indole Alkaloids. XVII. Five Dihydroindole Alkaloids from Aspidosperma Verbascifolium." Bulletin des Sociétés Chimiques Belges 78, no. 1-2 (September 2, 2010): 63–68. http://dx.doi.org/10.1002/bscb.19690780109.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Zhang, Lei, Fei Zhao, Mingyue Zheng, Yun Zhai, Jiang Wang, and Hong Liu. "ChemInform Abstract: Selective Synthesis of 5,6-Dihydroindolo[1,2-a]quinoxalines and 6,7-Dihydroindolo[2,3-c]quinolines by Orthogonal Copper and Palladium Catalysis." ChemInform 45, no. 6 (January 23, 2014): no. http://dx.doi.org/10.1002/chin.201406140.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Lyčka, Antonín, Josef Jirman, and Alois Koloničný. "15N, 13C, and 1H NMR Spectra of Azo and Hydrazo Compounds Derived from 1,3,3-Trimethyl-2-methylidene-2,3-dihydroindole (Fischer Base)." Collection of Czechoslovak Chemical Communications 63, no. 7 (1998): 1012–20. http://dx.doi.org/10.1135/cccc19981012.

Full text

Abstract:

The 15N, 13C, and 1H NMR spectra were measured for azo and hydrazo compounds derived from 1,3,3-trimethyl-2-methylidene-2,3-dihydroindole (Fischer base), which is a passive component with a terminal methylidene group. Products prepared by coupling in hydrochloric acid exist in the corresponding hydrazone form as the E-isomers. Neutralization gives a mixture of two isomeric azo compounds which differ in the arrangement at the C(2)=C(10) double bond. This mixture was alkylated with methyl iodide to obtain the =N-N(CH3)- hydrazone derivatives. The geometric isomers were resolved based on the NOESY approach and the stereospecific behaviour of the 2J(15N,13C) coupling constants was studied for the 15N-labelled compounds.

APA, Harvard, Vancouver, ISO, and other styles

27

He, Shuwen, Peng Li, Xing Dai, Hong Liu, Zhong Lai, Dong Xiao, Casey C. McComas, et al. "A general approach to access 5,6-dihydroindolo-naphthyridine ring system." Tetrahedron Letters 58, no. 14 (April 2017): 1373–75. http://dx.doi.org/10.1016/j.tetlet.2017.02.030.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Hashmi, A. Stephen K, Matthias Rudolph, Jan W Bats, Wolfgang Frey, Frank Rominger, and Thomas Oeser. "Gold-Catalyzed Synthesis of Chroman, Dihydrobenzofuran, Dihydroindole, and Tetrahydroquinoline Derivatives." Chemistry - A European Journal 14, no. 22 (July 28, 2008): 6672–78. http://dx.doi.org/10.1002/chem.200800210.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Carvajal-Miranda, Yendry, Roy Pérez-Salazar, and Jesús A. Varela. "Synthesis of Dihydroindolo[2,3-c]carbazole as Potential Telomerase Inhibitor." Journal of Heterocyclic Chemistry 53, no. 3 (May 27, 2015): 762–66. http://dx.doi.org/10.1002/jhet.2333.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

PREOBRAZHENSKAYA, M., A. KOROLEV, E. LAZHKO, L. ALEKSANDROVA, J. BERGMAN, and J. LINDSTROM. "Ascorbigen as a precursor of 5,11-dihydroindolo[3,2-b]carbazole." Food Chemistry 48, no. 1 (1993): 57–62. http://dx.doi.org/10.1016/0308-8146(93)90221-z.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Luo, Fen-Tair, and Ren-Tzong Wang. "Conversion of 2-Iodoaniline into (Z)-3-Methylene-2,3-dihydroindole Derivatives." HETEROCYCLES 32, no. 12 (1991): 2365. http://dx.doi.org/10.3987/com-91-5850.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Goldbrunner, Michael, Günther Loidl, Thomas Polossek, Albrecht Mannschreck, and Erwin von Angerer. "Inhibition of Tubulin Polymerization by 5,6-Dihydroindolo[2,1-a]isoquinoline Derivatives." Journal of Medicinal Chemistry 40, no. 22 (October 1997): 3524–33. http://dx.doi.org/10.1021/jm970177c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Ravishankar, T., K. Chinnakali, N. Arumugam, P. C. Srinivasan, Anwar Usman, and Hoong-Kun Fun. "2,5-Dimethyl-7-phenylsulfonyl-5,6-dihydroindolo[2,3-c]benzazepin-12-one." Acta Crystallographica Section E Structure Reports Online 61, no. 8 (July 6, 2005): o2410—o2412. http://dx.doi.org/10.1107/s1600536805020842.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Kilic, Haydar, Sinan Bayindir, and Nurullah Saracoglu. "4,7-Dihydroindole: A Synthon for the Preparations of 2-Substituted Indoles." Current Organic Synthesis 11, no. 2 (May 31, 2014): 167–81. http://dx.doi.org/10.2174/1570179411999140304102909.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

BASANAGOUDAR, L. D., C. S. MAHAJANSHETTI, and S. B. DAMBAL. "ChemInform Abstract: Synthesis of 7-Phenyl-5,6-dihydroindolo(1,2-a)quinoxalines." ChemInform 22, no. 47 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199147187.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Tholander, Joakim, and Jan Bergman. "Syntheses of 6,12-disubstituted 5,11-dihydroindolo[3,2-b]carbazoles, including 5,11-dihydroindolo[3,2-b]carbazole-6,12-dicarbaldehyde, an extremely efficient ligand for the TCDD (Ah) receptor." Tetrahedron 55, no. 43 (October 1999): 12577–94. http://dx.doi.org/10.1016/s0040-4020(99)00733-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Himbert, Gerhard, and Martin Ruppmich. "Eine Wagner-Meerwein-Umlagerung als Zwischenschritt bei der Dihydroindolon-Bildung aus 2-Diazo-acetoacetaniliden." Angewandte Chemie 102, no. 1 (January 1990): 69–70. http://dx.doi.org/10.1002/ange.19901020113.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Beller, Matthias, Claudia Breindl, Thomas H. Riermeier, Martin Eichberger, and Harald Trauthwein. "Basenkatalysierte Synthese vonN-(2-Arylethyl)anilinen und basenvermittelte Dominosynthese von 2,3-Dihydroindolen." Angewandte Chemie 110, no. 24 (December 17, 1998): 3571–73. http://dx.doi.org/10.1002/(sici)1521-3757(19981217)110:24<3571::aid-ange3571>3.0.co;2-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Reissig, Hans-Ulrich, and Virginie Blot. "Highly Substituted Dihydroindole Derivatives by Intermolecular Couplings of Samarium Ketyls and Indoles." Synlett 2006, no. 17 (October 2006): 2763–66. http://dx.doi.org/10.1055/s-2006-950285.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Kam, Toh-Seok, G. Subramaniam, Kuan-Hon Lim, and Yeun-Mun Choo. "Mersicarpine, an unusual tetracyclic dihydroindole alkaloid incorporating a seven-membered imine ring." Tetrahedron Letters 45, no. 31 (July 2004): 5995–98. http://dx.doi.org/10.1016/j.tetlet.2004.06.039.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Al-Kazwini, Akeel T., Peter O'Neill, Gerald E. Adams, Robert B. Cundall, Jean Maignan, and Alex Junino. "One-electron oxidation of 5,6-dihydroxy-2,3-dihydroindole: the influence of Zn2+." Journal of the Chemical Society, Perkin Transactions 2, no. 2 (1996): 241. http://dx.doi.org/10.1039/p29960000241.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Yeo, Seon-Ju, Hak Sung Kim, Suk Kim, Kee-In Lee, and Hyun Park. "Anticoccidial Effect of 3-(4-Methoxybenzylaminomethylene)-1,3-dihydroindole-2-one(5-108)." Yakhak Hoeji 59, no. 6 (December 31, 2015): 266–69. http://dx.doi.org/10.17480/psk.2015.59.6.266.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

VYSOTSKII, V. I., N. V. POLYAKOVA, O. V. KATERNOZA, V. V. ISAKOV, and L. I. SOKOLOVA. "ChemInform Abstract: Condensation of 3-Oxo-2-phenylimino-2,3-dihydroindole with Malonodinitrile." ChemInform 28, no. 17 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199717097.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Spyridonidou, Katerina, Manolis Fousteris, Marazioti Antonia, Athanasia Chatzianastasiou, Andreas Papapetropoulos, and Sotiris Nikolaropoulos. "Tricyclic indole and dihydroindole derivatives as new inhibitors of soluble guanylate cyclase." Bioorganic & Medicinal Chemistry Letters 19, no. 16 (August 2009): 4810–13. http://dx.doi.org/10.1016/j.bmcl.2009.06.047.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Himbert, Gerhard, and Martin Ruppmich. "A Wagner—Meerwein Rearrangement as Intermediate Step in the Formation of Dihydroindolones from 2-Diazoacetoacetanilides." Angewandte Chemie International Edition in English 29, no. 1 (January 1990): 86–87. http://dx.doi.org/10.1002/anie.199000861.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Tholander, Joakim, and Jan Bergman. "ChemInform Abstract: Syntheses of 6,12-Disubstituted 5,11-Dihydroindolo[3,2-b]carbazoles, Including 5,11-Dihydroindolo[3,2-b]carbazole-6,12-dicarbaldehyde, an Extremely Efficient Ligand for the TCDD (Ah) Receptor." ChemInform 31, no. 4 (June 11, 2010): no. http://dx.doi.org/10.1002/chin.200004133.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Jaisankar, Parasuraman, Bikash Pal, Ranjan K. Manna, Prasun K. Pradhan, S. Medda, Mukul K. Basu, and Venkatachalam S. Giri. "Synthesis of antileishmanial (5R)-(-)-5-carbomethoxy-3-formyl-5,6-dihydroindolo-[2,3-a]-indolizine." Arkivoc 2003, no. 9 (March 19, 2004): 150–57. http://dx.doi.org/10.3998/ark.5550190.0004.918.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Jeon, Kyu Ok, Ji Sook Yu, and Chang Kiu Lee. "Base-promoted rearrangements of ester groups in 3a,7a-dihydroindole-2,3,3a,4-tetraester." Journal of Heterocyclic Chemistry 44, no. 5 (September 2007): 1115–20. http://dx.doi.org/10.1002/jhet.5570440522.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

LUO, F. T., and R. T. WANG. "ChemInform Abstract: Conversion of 2-Iodoaniline into Z-3-Methylene-2,3-dihydroindole Derivatives." ChemInform 23, no. 16 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199216201.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

GOLDBRUNNER, M., G. LOIDL, T. POLOSSEK, A. MANNSCHRECK, and E. VON ANGERER. "ChemInform Abstract: Inhibition of Tubulin Polymerization by 5,6-Dihydroindolo[2,1-a]isoquinoline Derivatives." ChemInform 29, no. 7 (June 24, 2010): no. http://dx.doi.org/10.1002/chin.199807168.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!