Relevant bibliographies by topics / Indane derive

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  1. Journal articles

Academic literature on the topic 'Indane derive'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Indane derive"

1

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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2

Arnold, Donald R., Xinyao Du, and Kerstin M. Henseleit. "The effect of meta- and para-methoxy substitution on the reactivity of the radical cations of arylalkenes and alkanes. Radical ions in photochemistry. Part 26." Canadian Journal of Chemistry 69, no. 5 (1991): 839–52. http://dx.doi.org/10.1139/v91-124.

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The effect of meta- and para-methoxy substitution on the reactivity of some radical cations has been determined. The compounds chosen for study were 1-(3-methoxyphenyl)-1-phenylethylene (7), 1-(4-methoxyphenyl)-1-phenylethylene (8), 3-(3-methoxyphenyl)indene (9), 3-(4-methoxyphenyl)indene (10), methyl 2-(3-methoxyphenyl)-2-phenylethyl ether (11), methyl 2-(4-methoxyphenyl)-2-phenylethyl ether (12), cis- and trans-2-methoxy-1-(3-methoxyphenyl)indane (13), and cis- and trans-2-methoxy-1-(4-methoxyphenyl)indane (14). The radical cations of these compounds were generated by photosensitization (ele
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3

Abad, F., F. Álvarez, F. Fernández, X. García-Mera, and J. E. Rodríguez-Borges. "NEW CARBOCYCLIC NUCLEOSIDES DERIVED FROM INDAN." Nucleosides, Nucleotides and Nucleic Acids 20, no. 4-7 (2001): 1127–28. http://dx.doi.org/10.1081/ncn-100002503.

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4

Pio, Barbara, Harry R. Chobanian, Yan Guo, et al. "Design, synthesis and biological evaluation of indane derived GPR40 agoPAMs." Bioorganic & Medicinal Chemistry Letters 29, no. 14 (2019): 1842–48. http://dx.doi.org/10.1016/j.bmcl.2019.04.050.

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5

Deck, Paul A., and Carrie R. Maiorana. "Step−Growth Polymers Derived from Indene and Decafluorobiphenyl. A New Polymerization Mode for Indene." Macromolecules 34, no. 1 (2001): 9–13. http://dx.doi.org/10.1021/ma001424g.

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6

Darensbourg, Donald J., and Stephanie J. Wilson. "Synthesis of CO2-Derived Poly(indene carbonate) from Indene Oxide Utilizing Bifunctional Cobalt(III) Catalysts." Macromolecules 46, no. 15 (2013): 5929–34. http://dx.doi.org/10.1021/ma4013779.

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7

Kim, Ko Hoon, Se Hee Kim, Sunhong Park, and Jae Nyoung Kim. "Palladium-catalyzed synthesis of indane and cyclobuta[a]indenes from homoallylic alcohols derived from Baylis–Hillman adducts: base-dependent stereoselectivity for the benzylidene group in cyclobuta[a]indene." Tetrahedron 67, no. 19 (2011): 3328–36. http://dx.doi.org/10.1016/j.tet.2011.03.070.

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8

Abad, F., F. Alvarez, F. Fernandez, X. Garcia-Mera, and J. E. Rodriguez-Borges. "ChemInform Abstract: New Carbocyclic Nucleosides Derived from Indan." ChemInform 32, no. 49 (2010): no. http://dx.doi.org/10.1002/chin.200149213.

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9

Qian, Yimin, Karin Conde-Knape, Shawn D. Erickson, et al. "Potent MCH-1 receptor antagonists from cis-1,4-diaminocyclohexane-derived indane analogs." Bioorganic & Medicinal Chemistry Letters 23, no. 14 (2013): 4216–20. http://dx.doi.org/10.1016/j.bmcl.2013.05.017.

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10

Berezina, G. R., Yu G. Vorob'ev, and S. M. Vorob'eva. "Synthesis and Properties of Macroheterocycles Derived from an Indane-1,3-dione Analog." Russian Journal of General Chemistry 75, no. 12 (2005): 1946–48. http://dx.doi.org/10.1007/s11176-006-0019-x.

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