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Journal articles on the topic 'Indano'

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1

Junek, Hans, Manfred Klade, and Heinz Sterk. "�ber Dicyanmethylen-aminoindene, Indano-pyridazine und Indano-pyridine. Synthesen mit Nitrilen, 83. Mitt." Monatshefte f�r Chemie Chemical Monthly 120, no. 8-9 (1989): 781–88. http://dx.doi.org/10.1007/bf00809972.

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2

Palkó, Märta, Anasztäzia Hetényi, and Ferenc Fülöp. "Synthesis and stereochemistry of indano[1,2-d][1,3]oxazines and thiazines, new ring systems." Journal of Heterocyclic Chemistry 41, no. 1 (2004): 69–75. http://dx.doi.org/10.1002/jhet.5570410111.

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3

Arunprasath, Dhanarajan, Balasubramanian Devi Bala та Govindasamy Sekar. "Dictating the Reactivity of η3-Oxoallyl Pd-Intermediate toward 5-exo-trig Cyclization: Access to Indano-spirooxindoles". Journal of Organic Chemistry 83, № 18 (2018): 11298–308. http://dx.doi.org/10.1021/acs.joc.8b01891.

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4

Genest, David, Christophe Rochais, Cédric Lecoutey, et al. "Design, synthesis and biological evaluation of novel indano- and thiaindano-pyrazoles with potential interest for Alzheimer's disease." MedChemComm 4, no. 6 (2013): 925. http://dx.doi.org/10.1039/c3md00041a.

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5

Sarvesh, Pandey K., and Khan Nizamuddin. "Synthesis and Antimicrobial Study of Novel 1‐Aryl‐2‐oxo‐indano[3,2‐d]pyrido/pyrimido[1,2‐b]pyrimidines." Archiv der Pharmazie 341, no. 7 (2008): 418–23. http://dx.doi.org/10.1002/ardp.200700197.

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6

Mandal, Sudip Kumar. "INDANYL ANALOGS AS POTENTIAL ANTIMICROBIAL AGENTS." Asian Journal of Pharmaceutical and Clinical Research 11, no. 5 (2018): 278. http://dx.doi.org/10.22159/ajpcr.2018.v11i5.24635.

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Objective: The wide variety of biological activities of different indane derivatives makes them an interesting moiety in the field of medicinal chemistry. The objective of the study was to identify and develop novel antimicrobial agents from indanyl analogs.Methods: Recently synthesized indanyl analogs (4a-c and 5a-o) were examined against various pathogenic microorganisms (Gram-positive and Gram-negative bacteria and fungi) using serial dilution method. These analogs were found to possess antibacterial and antifungal activities with minimum inhibitory concentration values ranging between 1.56
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7

Bodwell, Graham, Ludger Ernst, Henning Hopf, and Peter G. Jones. "2,11-Dithia-[3.3](5,6)indano-orthocyclophane and 2,11-dithia-[3.3](5,6)indanocyclophane: synthesis, DNMR and X-ray structure analysis." Tetrahedron Letters 30, no. 44 (1989): 6005–8. http://dx.doi.org/10.1016/s0040-4039(01)93839-0.

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8

Suárez Bozo, Geraldine, María Sanguino Díaz, Gerardo Lucena, et al. "Agentes dopaminérgicos centrales análogos N-aralquil metoxilados del 2-aminoindano." Revista Colombiana de Ciencias Químico-Farmacéuticas 47, no. 2 (2018): 233–53. http://dx.doi.org/10.15446/rcciquifa.v47n2.73968.

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La neurotransmisión dopaminérgica interviene en los mecanismos que involucran los procesos motores, cognoscitivos, conductuales y neurocrinos y su mal funcionamiento la involucra en los trastornos neurodegenerativos que afectan al sistema nervioso central (SNC), tales como en la enfermedad de Parkinson y la enfermedad de Huntington, entre otras. Con el propósito de encontrar una solución terapéutica a estas patologías, en publicaciones anteriores hemos reportado la síntesis, la evaluación farmacológica y el estudio teórico computacional de los compuestos análogos mono y dihidroxilados (sobre e
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9

Silva, Ana L. R., Paula M. V. Gama, and Maria D. M. C. Ribeiro da Silva. "Influence of the functional groups −NH2, −OCH3, and −OH on the thermochemistry of indanes." Canadian Journal of Chemistry 97, no. 11 (2019): 788–94. http://dx.doi.org/10.1139/cjc-2019-0257.

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This work is a contribution to the thermochemical characterization of bicyclic hydrocarbons, reporting the study of six indane derivatives: 4-aminoindane, 5-aminoindane, 5-methoxyindane, 1-indanol, 2-indanol, and 5-indanol. The combustion calorimetry technique was used to measure the massic energy of combustion of each compound in the condensed state, which has been used to derive the corresponding standard (p° = 0.1 MPa) molar enthalpy of formation, at 298.15 K. The standard molar enthalpies of sublimation or vaporization of the compounds were determined by high-temperature Calvet microcalori
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10

Bøgesø, Klaus P., and Michael Bech Sommer. "The effect of aromatic substitution on neuroleptic activity in 1-piperazino-3-phenylindans. A comparison based on a new D-2 receptor model with corresponding 10-piperazino-10,11-dihydrodibenzo[b,f]thiepins." Collection of Czechoslovak Chemical Communications 56, no. 11 (1991): 2456–67. http://dx.doi.org/10.1135/cccc19912456.

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The validity of a new dopamine D-2 receptor interaction model based on conformational analysis and least-squares superimposition studies of the indan derivative tefludazine and the thiepin derivative octoclothepin was further tested by comparison of the effect of aromatic substitution on D-2 antagonistic activity in two series of indan and thiepin derivatives. The indan series include new derivatives substituted in the 4-, 7-, 2’- and 3’-position. The substitution effects were largely parallel with one important exception: Only 6-substituted indans have significant neuroleptic activity while b
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11

Balci, Neslihan, Latif Kelebekli, Suleyman Goksu, Baris Anil, and Ertan Sahin. "Synthesis and Characterisation of 2,3a,5,6,7a-pentaacetoxy-octahydro-1H-indene from indan-2-ol." Journal of Chemical Research 2009, no. 4 (2009): 248–51. http://dx.doi.org/10.3184/030823409x430211.

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A synthesis of 2,3a,5,6,7a-pentaacetoxyoctahydro-1 H-indene has been achieved starting from indan-2-ol. The Birch reduction of indan-2-ol gave 4,7-dihydro-2-indanol in high yield which when followed by acetylation, resulted in the corresponding acetates. The OsO4 oxidation of the 2-acetoxy-4,7-dihydroindane followed by acetylation furnished the desired pentaacetates in high yield.
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12

Francos, Javier, Sergio E. García-Garrido, Javier Borge, Francisco J. Suárez, and Victorio Cadierno. "Butadiene dyes based on 3-(dicyanomethylidene)indan-1-one and 1,3-bis(dicyanomethylidene)indane: synthesis, characterization and solvatochromic behaviour." RSC Advances 6, no. 9 (2016): 6858–67. http://dx.doi.org/10.1039/c5ra27005g.

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Novel 1,1-diaryl-substituted butadiene dyes containing 3-(dicyanomethylidene)indan-1-one and 1,3-bis(dicyanomethylidene)indane have been synthetized, and their light absorption and solvatochromic properties evaluated.
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13

Khan, Salman A., Abdullah M. Asiri, and Saad H. Al-Thaqafy. "Optical properties and fluorescence quenching of biologically active ethyl 4-(4-N,N-dimethylamino phenyl)-2-methyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate (DDPC) dye as a probe to determine CMC of surfactants." RSC Advances 6, no. 104 (2016): 102218–25. http://dx.doi.org/10.1039/c6ra02814d.

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4-(4-N,N-Dimethylamino phenyl)-2-methyl-5-oxo-4,5-dihydro-1H-indeno[1,2-b]pyridine-3-carboxylate (DDPC) was prepared via the multi-component reaction of indane-1,3-dione with 4-(dimethylamino)benzaldehyde, ethyl acetoacetate and ammonium acetate.
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14

Mączka, Wanda, Katarzyna Wińska, Małgorzata Grabarczyk, and Renata Galek. "Plant-Mediated Enantioselective Transformation of Indan-1-One and Indan-1-ol." Catalysts 9, no. 10 (2019): 844. http://dx.doi.org/10.3390/catal9100844.

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The main purpose of this work was to discover the way to obtain pure enantiomers of indan-1-ol. The subject of the study was the ability of the plant enzyme system to reduce the carbonyl group of indan-1-one, as well as to oxidize the hydroxyl group of racemic indan-1-ol. Locally available fruit and vegetables were selected for stereoselective biotransformation. During the reduction, mainly alcohol of the S-(+)-configuration with a high enantiomeric excess (ee = 99%) was obtained. The opposite enantiomer was obtained in bioreduction with the apple and parsley. Racemic indan-1-ol was oxidized b
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15

Soto Rueda, Eliana Marcela, Yenni Leandra Rodríguez Ruiz, Nelsy Loango Chamorro, and Patricia Landázuri. "Extractos de Tagetes patula L. (Asteraceae): un potencial bactericida contra el Moko." Revista Mexicana de Ciencias Agrícolas 9, no. 5 (2018): 949–59. http://dx.doi.org/10.29312/remexca.v9i5.1504.

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Ralstonia solanacearum raza 2 es la causante del Moko o marchitez bacteriana, produciendo grandes pérdidas económicas en cultivos como plátano, tabaco y tomate. Se han descrito varios componentes de los extractos y del aceite esencial (AE) de Tagetes patula L., que incluyen: benzofuranos, carotenoides, flavonoides y tiofenos que son biológicamente activos y potencialmente alelopáticos contra muchos organismos patógenos. Las investigaciones del efecto de los extractos y el AE de T. patula L contra R. solanacearum son escasas. El objetivo de esta investigación fue analizar el potencial antioxida
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16

Fies, Martin, and Klaus Friedrich. "Kohlenstoff-analoge Strukturen von Brasilin und H�matoxylin vom Indeno[1,2-?] indan-Typ." Journal f�r Praktische Chemie/Chemiker-Zeitung 337, no. 1 (1995): 596–98. http://dx.doi.org/10.1002/prac.199533701125.

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17

Sharma, Himanshu, Priyank Kumar Sharma, and Soumyajit Das. "Revisiting indeno[2,1-c]fluorene synthesis while exploring the fully conjugated s-indaceno[2,1-c:6,5-c′]difluorene." Chemical Communications 56, no. 76 (2020): 11319–22. http://dx.doi.org/10.1039/d0cc04418k.

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18

Shukla, Upendra K., Raieshwar Singh, J. M. Khanna, et al. "Synthesis of trans-2-[N-(2-Hydroxy-1,2,3,4-tetrahydronaphthalene-1-yl)]iminothiazolidine and Related Compounds - A New Class of Antidepressants." Collection of Czechoslovak Chemical Communications 57, no. 2 (1992): 415–24. http://dx.doi.org/10.1135/cccc19920415.

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Antiparasitic and antidepressant activities exhibited by tetramisole (I) and its enantiomers prompted the study of its structural analogs trans-2-[N-(2-hydroxy-1,2,3,4-tetrahydronaphthalene/indane-1-yl)]iminothiazolidine (VIII/IX) and 2,3,4a,5,6,10b-hexahydronaphtho[1',2':4,5]-imidazo[2,1-b]thiazole (XII), 2,3,4a,5-tetrahydro-9bH-indeno[1',2':4,5]imidazo[2,1-b]thiazole (XIII), and 2,3,4a,5-tetrahydro-9bH-indeno[1',2':4,5]imidazo[2,1-b]thiazole (XVI), and a homolog 3,4,6,7-tetrahydro-7-phenyl-2H-imidazo[2,1-b]-1,3-thiazine (XX). While none of these compounds showed any noteworthy antiparasitic
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19

Mitrochkine, Anton, Franck Eydoux, Monique Martres, Gérard Gil, Andreas Heumann, and Marius Réglier. "Synthesis of enantiomerically pure (1S, 2R)-epoxy indane and cis-(1R,2S)-2-amino-1-indanol." Tetrahedron: Asymmetry 6, no. 1 (1995): 59–62. http://dx.doi.org/10.1016/0957-4166(94)00351-b.

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20

Rao, V. Rajeswar, and P. Vijaya Kumar. "A Facile One Step Synthesis of 3-(2-oxo-2H-chromen-3-yl)-indeno-[2,1-c]pyridazin-9-one." Journal of Chemical Research 2005, no. 4 (2005): 267–69. http://dx.doi.org/10.3184/0308234054213447.

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3-Acetylcoumarins (1) on reaction with ninhydrin (2) in acetic acid followed by treatment of in situ formed 2-hydroxy-2-[2-oxo-2-(2-oxo-2H-chromen-3-yl)-ethyl]indan-1,3-diones (3) with hydrazine hydrate resulted in the formation of corresponding 3-(2-oxo-2H-chromen-3-yl)-indeno[2,1-c]pyridazin-9-ones (4) in a single step with an excellent yields. The structures of newly synthesised compounds (4) were confirmed by unambiguous synthesis involving a two step process from 3-acetylcoumarins.
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21

FIES, M., та K. FRIEDRICH. "ChemInform Abstract: Carbon Analogous Structures of Brazilin and Hematoxylin of the Indeno( 1,2-α)indan Type." ChemInform 27, № 6 (2010): no. http://dx.doi.org/10.1002/chin.199606198.

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22

Dehghanpour, Hamid Reza, Mohammad H. Mosslemin, and Razieh Mohebat. "Graphene Oxide: A Carbocatalyst for the One-Pot Multicomponent Synthesis of 5-Aryl-1H-Indeno[2’,1’:5,6]Pyrido[2,3-d]Pyrimidine-2,4,6(3H)-Trione." Journal of Chemical Research 42, no. 1 (2018): 35–39. http://dx.doi.org/10.3184/174751918x15161933697835.

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A simple, straightforward and efficient method is described for the synthesis of 5-aryl-1H-indeno[2’,1’:5,6]pyrido[2,3-d]pyrimidine-2,4,6(3H)-trione via one-pot multicomponent reaction of indane-1,3-dione, arylaldehydes and 6-aminopyrimidin-2,4(1H,3H)-dione in presence of catalytic amount of graphene oxide in water. Graphene oxide is a versatile carbocatalyst and this is the first report on its application in a pyrido[2,3-d]pyrimidine synthesis. Good yield, use of readily available starting materials, operational simplicity, easy work-up and eco-friendly re-usable catalyst are the key features
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23

ALESSO, E. N., D. G. TOMBARI, A. F. IBANEZ, G. Y. MOLTRASIO IGLESIAS, and J. M. AGUIRRE. "ChemInform Abstract: Synthesis and NMR Spectroscopy of Indan Structures: Indans Mono- and Disubstituted in the Pentagonal Ring." ChemInform 22, no. 48 (2010): no. http://dx.doi.org/10.1002/chin.199148039.

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24

Das, Aloke, K. K. Mahato, Sujit S. Panja, and Tapas Chakraborty. "Conformations of indan and 2-indanol: A combined study by UV laser spectroscopy and quantum chemistry calculation." Journal of Chemical Physics 119, no. 5 (2003): 2523–30. http://dx.doi.org/10.1063/1.1587111.

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25

Stadlbauer, Wolfgang, and Michaela Fischer. "Thermal cyclization of 3-azido-2-phenyl-indan-l-one to 5h-indeno[1,2-b]indol-10-one." Journal of Heterocyclic Chemistry 39, no. 1 (2002): 131–35. http://dx.doi.org/10.1002/jhet.5570390119.

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26

MITROCHKINE, A., F. EYDOUX, M. MARTRES, G. GIL, A. HEUMANN, and M. REGLIER. "ChemInform Abstract: Synthesis of Enantiomerically Pure (1S,2R)-Epoxy Indan and cis-(1R,2S)- 2-Amino-1-indanol." ChemInform 26, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199527055.

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27

Zarl, Elisabeth, Jörg H. Albering, Roland C. Fischer, et al. "Tin-containing Indane and Tetralin Derivatives." Zeitschrift für Naturforschung B 64, no. 11-12 (2009): 1591–97. http://dx.doi.org/10.1515/znb-2009-11-1244.

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The preparation of tin-containing indane and tetralin derivatives via two different reaction pathways is reported. The first route is the reaction of dichlorostannanes or bis(fluoroalkylsulfonyl)stannanes withα,α'-di(chloromagnesium)xylene. The second reaction is the direct coupling of chlorostannanes and α,α'-dichloroxylene which always yields a mixture of tin-containing indanes and tetralins. The separation of these compounds can easily be achieved by fractional crystallization. By these simple and effective routes the first 2,3-distannatetralins were synthesized
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28

Borie, Cyril, Lutz Ackermann, and Malek Nechab. "Enantioselective syntheses of indanes: from organocatalysis to C–H functionalization." Chemical Society Reviews 45, no. 5 (2016): 1368–86. http://dx.doi.org/10.1039/c5cs00622h.

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The indanyl core is ubiquitous in a large variety of drugs and natural products. Remarkable recent progress has been accomplished in the step-economical assembly of functionalization of chiral indanes by means of enantioselective catalysis, with major progress being achieved in organocatalysis and C–H activation chemistry.
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29

Maiuolo, Loredana, Vincenzo Algieri, Beatrice Russo, et al. "Synthesis, Biological and In Silico Evaluation of Pure Nucleobase-Containing Spiro (Indane-Isoxazolidine) Derivatives as Potential Inhibitors of MDM2–p53 Interaction." Molecules 24, no. 16 (2019): 2909. http://dx.doi.org/10.3390/molecules24162909.

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Nucleobase-containing isoxazolidines spiro-bonded to an indane core have been synthesized in very good yields by regio- and diastereoselective 1,3-dipolar cycloaddition starting from indanyl nitrones and N-vinylnucleobases by using environmentally benign microwave technology. The contemporary presence of various structural groups that are individually active scaffolds of different typology of drugs, has directed us to speculate that these compounds may act as inhibitors of MDM2–p53 interaction. Therefore, both computational calculations and antiproliferative screening against A549 human lung a
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30

HeeJung Kim. "Notturno Indiano." Journal of Mediterranean Area Studies 16, no. 2 (2014): 65–70. http://dx.doi.org/10.18218/jmas.2014.16.2.65.

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31

Ferraro, Bruno, Antonio Tabucchi, and Anna Dolfi. "Notturno indiano." Modern Language Review 93, no. 1 (1998): 247. http://dx.doi.org/10.2307/3733714.

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32

Aamouche, A., and P. J. Stephens. "Conformational Analysis in Solution of a Chiral Bisoxazoline Molecule: Vibrational Circular Dichroism Spectroscopy and Density Functional Theory Study." International Journal of Spectroscopy 2011 (December 5, 2011): 1–11. http://dx.doi.org/10.1155/2011/905045.

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The conformations of the chiral bisoxazoline: 2,2′-methylenebis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole] (also named IndaBOX), have been studied. Density functional theory (DFT) calculations identify four inequivalent stable conformations. Two, I and II have, C2 symmetry; two, III and IV, have C1 symmetry. The electronic energies of I–IV are ordered: I<II<III<IV. The span in energy is <1.0 kcal/mole. Vibrational unpolarised absorption and circular dichroism spectra have been predicted for the four conformations using DFT. Comparison of population-weighted spectra to experimental spec
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33

Alesso, Elba N., Dora G. Tombari, Adriana F. Ibañez, Graciela Y. Moltrasio Iglesias, and José M. Aguirre. "Synthesis and nuclear magnetic resonance spectroscopy of indane structures: indanes mono- and disubstituted in the pentagonal ring." Canadian Journal of Chemistry 69, no. 7 (1991): 1166–70. http://dx.doi.org/10.1139/v91-174.

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Indanes monosubstituted and 1,2- and 1,3-disubstituted in the pentagonal ring were synthesized, and configurations were assigned to the 1,2-disubstituted compounds by means of nuclear magnetic resonance spectroscopy. Key words: mono- and disubstituted indanes, conformation, configuration, 1H and 13C NMR, synthesis.
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34

Chan, Kit, Neil Frankish, Tao Zhang, et al. "Bioactive indanes: insight into the bioactivity of indane dimers related to the lead anti‐inflammatory molecule PH46A." Journal of Pharmacy and Pharmacology 72, no. 7 (2020): 927–37. http://dx.doi.org/10.1111/jphp.13269.

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35

Tatsugi, Jiro, and Yasuji Izawa. "A Convenient One-Pot Synthesis of Indane-1,2,3-triones by Oxidation of Indan-1-ones with N-Bromosuccinimide-dimethyl Sulfoxide Reagent." Synthetic Communications 28, no. 5 (1998): 859–64. http://dx.doi.org/10.1080/00032719808006484.

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36

Krasnaya, Zh A., E. O. Tret’yakova та S. G. Zlotin. "Reactions of β-dimethylaminoacrolein aminal and 3-dimethylamino-1,1,3-trimethoxypropane with 3-(dicyanomethylidene)indan-1-one and 1,3-bis(dicyanomethylidene)indane". Russian Chemical Bulletin 56, № 11 (2007): 2258–62. http://dx.doi.org/10.1007/s11172-007-0355-y.

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37

Frank, Daniel, Constanze Langer, Steffi Hußlein, Peter Klein, and Henrik Rieß. "inDAgo-Helfer-App." i-com 13, no. 3 (2014): 43–51. http://dx.doi.org/10.1515/icom.2014.0029.

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Zusammenfassung Im Projekt inDAgo entwickeln Forschungspartner eine Lösung, die Senioren in Darmstadt bei ihrer täglichen Mobilität unterstützt. Dabei soll ein Netzwerk von freiwilligen Helfern bereit stehen, um den Senioren bei Problemen auf ihren täglichen Wegen zur Hand zu gehen. Koordiniert werden sollen die Helfer über eine Smartphone- Applikation. Der folgende Artikel beschreibt die Entwicklung von Konzept und Prototyp für diese Applikation im Rahmen einer Masterarbeit. Einen Schwerpunkt bildete hierbei die Frage, wie man Helfer motivieren kann. Dafür kam der benutzerzentrierte Gestaltun
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38

Keen, Benjamin. "Derecho indiano. Estudios." Hispanic American Historical Review 73, no. 1 (1993): 148. http://dx.doi.org/10.1215/00182168-73.1.148.

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39

Abdourazak, Atteye H., Zbigniew Marcinow, Andrzej Sygula, Renata Sygula, and Peter W. Rabideau. "Buckybowls 2. Toward the Total Synthesis of Buckminsterfullerene (C60): Benz[5,6]-as-indaceno[3,2,1,8,7-mnopqr]indeno[4,3,2,1-cdef]chrysene." Journal of the American Chemical Society 117, no. 23 (1995): 6410–11. http://dx.doi.org/10.1021/ja00128a052.

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40

Zende, Vidya, Tejpalsingh Ramsingh Girase, Nicolas Chrysochos, Anant Ramakant Kapdi, and Carola Schulzke. "Crystal structure of 1-butyl-3-{2-[(indan-5-yl)amino]-2-oxoethyl}-1H-imidazol-3-ium chloride." Acta Crystallographica Section E Crystallographic Communications 74, no. 11 (2018): 1665–68. http://dx.doi.org/10.1107/s2056989018014792.

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In the cation of the title molecular salt, C18H24N3O+·Cl−, an intramolecular C—H...O hydrogen bond stabilizes the almost coplanar orientation of the aromatic ring of the indane unit and the amide plane. In the crystal, the packing is dominated by intermolecular C—H...Cl hydrogen-bonding interactions that result in the formation of slab-like structures propagating along [010]. The slabs are linked by weak C—H...O interactions, forming layers lying parallel to (100). The methylene carbon atom of the indanyl substituent is disordered over two positions with a refined occupancy ratio of 0.84 (2):0
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41

Chougule, Uttam B., Hemant V. Chavan, and Savita R. Dhongade. "Synthesis, Characterization and Biological Evaluation of Some 2-[1-(1,3-Diphenyl-1HPyrazol-4-yl)-meth-(E)-ylidene]indan-1-one Derivatives as Antibacterial Agents." Asian Journal of Organic & Medicinal Chemistry 5, no. 2 (2020): 127–32. http://dx.doi.org/10.14233/ajomc.2020.ajomc-p258.

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A new series of 2-[1-(1,3-diphenyl-1H-pyrazol-4-yl)-meth-(E)-ylidene]-indan-1-one derivatives (5a-l) have been synthesized through through the Knoevenagel condensation of pyrazole carbaldehydes with differently substituted 1-indanone derivatives in the presence of base. A high yielding and solvent-free method was developed for the synthesis of hydrazones from acetophenones under microwave irradiation in a very short reaction time. Structures of the newly synthesized compounds were affirmed by IR, 1H & 13C NMR and mass spectroscopic analysis. The confirmed structures were screened for their
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TATSUGI, J., and Y. IZAWA. "ChemInform Abstract: A Convenient One-Pot Synthesis of Indane-1,2,3-triones by Oxidation of Indan-1-ones with N-Bromosuccinimide-dimethyl Sulfoxide Reagent." ChemInform 29, no. 24 (2010): no. http://dx.doi.org/10.1002/chin.199824095.

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Basadre Ayulo, Jorge. "Consideraciones sobre derecho indiano." Ius et Praxis, no. 017 (1991): 261–71. http://dx.doi.org/10.26439/iusetpraxis1991.n017.3470.

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Hampe-Martinez, Teodoro, Ismael Sanchez Bella, Alberto de la Hera, and Carlos Diaz Rementeria. "Historia del Derecho Indiano." Hispanic American Historical Review 74, no. 1 (1994): 140. http://dx.doi.org/10.2307/2517453.

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Kempter, G., M. Schwalba, W. Stoß, and K. Walter. "Azpentalene aus Indeno-indolen." Zeitschrift für Chemie 2, no. 8 (2010): 252. http://dx.doi.org/10.1002/zfch.19620020804.

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Hampe-Martínez, Teodoro. "Historia del Derecho Indiano." Hispanic American Historical Review 74, no. 1 (1994): 140–41. http://dx.doi.org/10.1215/00182168-74.1.140.

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ALADOS-ARBOLEDAS, L., H. HORVATH, G. PAVESE, et al. "INDALO 2003 FIELD CAMPAIGN." Journal of Aerosol Science 35 (July 2004): S981—S982. http://dx.doi.org/10.1016/j.jaerosci.2004.06.050.

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Jeon, Ki Joon, and Kee-Jung Lee. "Synthesis of 4H-indeno[1,2-b]thiophenes, 8H-indeno[2,1-b]-thiophenes and 8H-indeno[2,1-b]furans having acrylic acid unit." Journal of Heterocyclic Chemistry 45, no. 2 (2008): 615–19. http://dx.doi.org/10.1002/jhet.5570450252.

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ABDOURAZAK, A. H., Z. MARCINOW, A. SYGULA, R. SYGULA, and P. W. RABIDEAU. "ChemInform Abstract: Buckybowls. Part 2. Toward the Total Synthesis of Buckminsterfullerene (C60): Benz(5,6)-as-indaceno(3,2,1,8,7-mnopqr)indeno(4,3,2,1-cdef) chrysene." ChemInform 26, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199540121.

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Turner, Alan B., and William T. A. Harrison. "2-(4-Ethoxybenzyl)indan." Acta Crystallographica Section E Structure Reports Online 60, no. 11 (2004): o2138—o2139. http://dx.doi.org/10.1107/s1600536804026492.

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