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

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Published: 4 June 2021
Last updated: 19 February 2022

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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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3

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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11

Schlemper, E. O., M. M. Nikaido, and G. R. Clark. "The relative configuration of 8-[(2,2-dimethyl-3-oxocyclohexyl)methoxymethyl]-1-methylbicyclo[4.2.0]octan-7-one." Acta Crystallographica Section C Crystal Structure Communications 43, no. 9 (1987): 1742–45. http://dx.doi.org/10.1107/s0108270187090334.

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12

Fair, C. K., G. R. Clark, and M. M. Nikaido. "The relative configuration of 8-[(2,2-dimethyl-3-oxocyclohexyl)hydroxymethyl]-1-methylbicyclo[4.2.0]octan-7-one, C18H28O3." Acta Crystallographica Section C Crystal Structure Communications 41, no. 1 (1985): 155–57. http://dx.doi.org/10.1107/s0108270185003122.

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13

Banwell, Martin G., Malcolm D. McLeod, and Andrew G. Riches. "Taxane Diterpene Synthesis Studies. Part 2: Towards Taxinine—Enantiospecific Construction of an AB-ring Substructure Incorporating both Quaternary Carbon Centres and Attempts to Annulate the C-ring." Australian Journal of Chemistry 57, no. 1 (2004): 53. http://dx.doi.org/10.1071/ch03161.

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In connection with efforts to develop an efficient total synthesis of the biologically active natural product taxinine 1, the enzymatically-derived and monochiral cis-1,2-dihydrocatechol 7 was converted, over several steps including a Diels–Alder cycloaddition reaction, into the bicyclo[2.2.2]octan-2-one 18. Reaction of the last compound with the organocerium reagent 22 afforded the 1,5-diene 23 which engaged in an anionic oxy-Cope rearrangement reaction to give, after C-methylation of the product enolate 25, bicyclo[5.3.1]undecenone 27 embodying the AB-ring system of target 1. Two methods for
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14

Singh, Pradeep N. D., Jana Pika, Jeanette A. Krause Bauer, and Anna D. Gudmundsdóttir. "3′-Isopropyl-8′,8′-dimethyl-2-benzofuran-1-spiro-7′-bicyclo[4.2.0]octa-1′(6′),2′,4′-trien-3-one." Acta Crystallographica Section E Structure Reports Online 60, no. 12 (2004): o2390—o2392. http://dx.doi.org/10.1107/s160053680402940x.

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15

Hu, Xiao Yi, Dang Quan Zhang, and Lin Lin Guo. "Py-GC/MS Analysis of Bioactive Components of 550°C Pyrolyzate from Acetone Extractives of Cinnamomum camphora Root Wood." Key Engineering Materials 480-481 (June 2011): 478–83. http://dx.doi.org/10.4028/www.scientific.net/kem.480-481.478.

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The researches are very less about the acetone extractives of rood wood from Cinnamomum camphora, a famous non-wood tree in China. Therefore, 550°C-based Py-GC/MS was used to analyze the high-grade resource recovering approaches of C. camphora root wood. The analytical result showed that the main components of the acetone extractives of C. camphora root wood by 550°C-based pyrolysis- GC/MS are as: Decanoic acid, 1,2,3-propanetriyl ester (16.720%), 4-Nitrophenyl laurate (9.104%), 1,3-Benzodioxole, 5-(2-propenyl)- (6.3744%), Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)- (5.646%), 2-Hydroxy
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16

Masciocchi, N., A. Aulisio, G. Bertolini, M. Sada, F. Garis, and L. Malpezzi. "Disclosing the extensive crystal chemistry of Ivabradine hydrochloride, in its pure and solvated phases." Powder Diffraction 28, no. 3 (2013): 200–206. http://dx.doi.org/10.1017/s0885715613000365.

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Powder diffraction data are presented for Ivabradine hydrochloride (pure and solvated forms), a drug marketed worldwide for symptomatic treatment of angina pectoris and inappropriate sinus tachycardia. [Ivrabradine: 3-[3-({[(7S)-3,4-dimethoxy bicyclo[4.2.0]octa-1,3,5-trien-7-yl]methyl}(methyl)amino)propyl]-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepin-2-one]. Many are the different (polymorphic or solvated) phases claimed in the scientific or forensic literature. We have here prepared monophasic samples of six different ivabradine hydrochloride species. Exposure to water vapours, at room te
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17

Werstiuk, Nick Henry, Gwen Irene Wade, and Peter John Joseph Martin. "Facile H–D exchange of the bridgehead methyls of bicyclo[2.2.2]octan-2,5-diones. Evidence for a carbon analogue of the acyloin rearrangement." Canadian Journal of Chemistry 63, no. 9 (1985): 2582–83. http://dx.doi.org/10.1139/v85-428.

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Hexamethyltwistyl-2,5-dione 4 has been synthesized and its H–D exchange studied in t-BuOK/t-BuOD at 125 °C. We find that the bridgehead methyl at C-3 undergoes exchange 7 × 105 times faster than the bridgehead methyl of bicyclo[2.2.1]heptan-2-one (fenchone). This result, along with a previous study, establishes the first examples of the carbon analogue of the acyloin rearrangement of alicyclic systems.
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18

"7-CHLORO-7-CYANOBICYCLO[4.2.0]OCTAN-8-ONE." Organic Syntheses 69 (1990): 205. http://dx.doi.org/10.15227/orgsyn.069.0205.

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19

FISHBEIN, P. L., and H. W. MOORE. "ChemInform Abstract: 7-Chloro-7-cyanobicyclo(4.2.0)octan-8-one (Prepared from Chlorocyanoketene)." ChemInform 21, no. 22 (1990). http://dx.doi.org/10.1002/chin.199022118.

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20

COTTERILL, I. C., H. FINCH, D. P. REYNOLDS, et al. "ChemInform Abstract: 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." ChemInform 19, no. 37 (1988). http://dx.doi.org/10.1002/chin.198837171.

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21

FAYTER, J. A., L. D. CAMA, B. G. CHRISTENSEN, and J. HIRSHFIELD. "ChemInform Abstract: Synthetic Carbapenem Antibiotics. Part 2. Stereoisomers of 7-Hydroxyethyl-2,2,5- trimethyl-3-oxa-1-azabicyclo[4.2.0]octan-8-one. Part 3. 1-Methyl Thienamycin." Chemischer Informationsdienst 16, no. 24 (1985). http://dx.doi.org/10.1002/chin.198524373.

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