Relevant bibliographies by topics / Bicyclo[4.2.0]octan-7-one

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  2. Dissertations / Theses

Academic literature on the topic 'Bicyclo[4.2.0]octan-7-one'

Author: Grafiati
Published: 4 June 2021
Last updated: 19 February 2022

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Journal articles on the topic "Bicyclo[4.2.0]octan-7-one"

1

Tinant, B., J. P. Declercq, and B. Gobeaux. "8-(N-Methyl-N-p-tolylsulfonylamino)bicyclo[4.2.0]octan-7-one." Acta Crystallographica Section C Crystal Structure Communications 46, no. 10 (1990): 1944–46. http://dx.doi.org/10.1107/s0108270190003936.

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2

Wu, Helen Y., Keith A. M. Walker, and Janis T. Nelson. "Enolate reactions of bicyclo[4.2.0]octan-7-ones." Journal of Organic Chemistry 55, no. 17 (1990): 5074–78. http://dx.doi.org/10.1021/jo00304a020.

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WU, H. Y., K. A. M. WALKER, and J. T. NELSON. "ChemInform Abstract: Enolate Reactions of Bicyclo(4.2.0)octan-7-ones." ChemInform 22, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199108165.

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4

Argay, Gyula, László Fábián, Alajos Kálmán, Gábor Bernáth, and Zsuzsanna Cs Gyarmati. "cis-7-Azabicyclo[4.2.0]octan-8-one." Acta Crystallographica Section E Structure Reports Online 60, no. 2 (2004): o170—o172. http://dx.doi.org/10.1107/s1600536803027958.

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5

Fishbein, Paul L., and Harold W. Moore. "7-Chloro-7-cyanobicyclo[4.2.0]octan-8-one (Prepared from Chlorocyanoketene)." Synthetic Communications 19, no. 19 (1989): 3283–87. http://dx.doi.org/10.1080/00397918908052730.

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6

Ngamga, Dieudonne, Josephine Bipa, Pearl Lebatha, et al. "Isoquinoline Alkaloids and Homoisoflavonoids from Drimiopsis barteri Bak and D. burkei Bak." Natural Product Communications 3, no. 5 (2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300518.

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The powdered bulbs and leaves of Drimiopsis barteri yielded two novel isoquinoline alkaloids: 5-hydroxy-7,2′,3′,4′-tetramethoxy{2H-1-}benzopyran [4,3-c]isoquinoline and 6-hydroxy-7,2′,3′,4′-tetramethoxy{2H-1-}benzopyran [4,3-c]isoquinoline, three new scillascillins: 5,7-dihydroxy-2′,3′,4′-trimethoxyspiro-{2H-1-benzopyran-7′-bicyclo [4.2.0]octa[1,3,5]-triene}-4-one, 5-hydroxy-7,2′,3′,4′-tetramethoxyspiro{2H-1-benzopyran-7′-bicyclo [4.2.0]octa[1,3,5]-triene}-4-one and 5,2′,4′-trihydroxy-7,3′-dimethoxyspiro{2H-1-benzopyran-7′-bicyclo [4.2.0]octa[1,3,5]-triene}-4-one, and a tetrahydroxyhomo-isofla
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7

Wu, Helen Y., Keith A. M. Walker, and Janis T. Nelson. "Stereochemical Consequences of 6- and 8-Substitution in Reactions of Bicyclo[4.2.0]octan-7-ones." Journal of Organic Chemistry 59, no. 6 (1994): 1389–95. http://dx.doi.org/10.1021/jo00085a031.

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8

WU, H. Y., K. A. M. WALKER, and J. T. NELSON. "ChemInform Abstract: Stereochemical Consequences of 6- and 8-Substitution in Reactions of Bicyclo(4.2.0)octan-7-ones." ChemInform 25, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199433140.

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9

Cotterill, Ian C., Harry Finch, Derek P. Reynolds, et al. "Enzymatic resolution of bicyclo[4.2.0]oct-2-en-7-ol and the preparation of some polysubstituted bicyclo[3.3.0]octan-2-ones via highly strained tricyclo[4.2.0.01,5]octan-8-ones." Journal of the Chemical Society, Chemical Communications, no. 7 (1988): 470. http://dx.doi.org/10.1039/c39880000470.

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10

Toivola, Reijo J., Satu K. Savilampi, and Ari M. P. Koskinen. "The first direct synthesis of bicyclo[4.2.0]oct-1(6)-en-7-one." Tetrahedron Letters 41, no. 32 (2000): 6207–10. http://dx.doi.org/10.1016/s0040-4039(00)01009-1.

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Dissertations / Theses on the topic "Bicyclo[4.2.0]octan-7-one"

1

Ozer, Melek Sermin. "Functionalization Of Saturated Bicyclic Hydrocarbons: High Temperature Bromination." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12612938/index.pdf.

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Abstract:
ABSTRACT FUNCTIONALIZATION OF SATURATED BICYCLIC HYDROCARBONS: HIGH TEMPERATURE BROMINATION &Ouml<br>zer, Melek Sermin M.Sc., Department of Chemistry Supervisor: Prof. Dr. Metin Balci January 2011, 139 pages Although hydrocarbons are readily available and extremely cheap starting materials, they cannot be used in synthetic chemistry without prior activation. The selective functionalization of saturated hydrocarbons under mild conditions is of both biochemical and industrial importance. Initially, saturated hydrocarbons such as octahydro-1H-indene 80, octahydro-1H-4,7-methanoindene 81 a
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