Relevant bibliographies by topics / Bicyclo[4.3.1]decanone

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Bicyclo[4.3.1]decanone'

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

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Journal articles on the topic "Bicyclo[4.3.1]decanone"

1

Abboud, K. A., Y. Xie, and E. J. Enholm. "A cis-Fused Decalone and a Bicyclo[4.3.1]decanone Ring System." Acta Crystallographica Section C Crystal Structure Communications 52, no. 7 (1996): 1829–31. http://dx.doi.org/10.1107/s0108270196000121.

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2

ABBOUD, K. A., Y. XIE, and E. J. ENHOLM. "ChemInform Abstract: A cis-Fused Decalone and a Bicyclo(4.3.1)decanone Ring System." ChemInform 27, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199645044.

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3

Bernhardt, Paul V., Raymond M. Carman, and Roger P. C. Derbyshire. "The Reaction of 8-Amino-p-menthene Derivatives with Electrophiles." Australian Journal of Chemistry 57, no. 6 (2004): 583. http://dx.doi.org/10.1071/ch03158.

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Attempts to ring-close the nitrogen atom of 8-amino-p-menth-1-ene and of N-substituted 8-amino-p-menth-1-enes onto the C1–C2 double-bond carbons has led to a range of bicyclo[2.2.2] and bicyclo[3.2.1] products, together with the novel bicyclo[4.3.1]-1,3-oxazepine 9.
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4

Huters, Alexander D., Evan D. Styduhar, and Neil K. Garg. "Totalsynthesen der Welwitindolinone mit Bicyclo[4.3.1]-Kern." Angewandte Chemie 124, no. 16 (2012): 3820–28. http://dx.doi.org/10.1002/ange.201107567.

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5

Kreiter, Cornelius G., та Klaus Lehr. "Photochemische Reaktionen von Übergangsmetall-Organyl-Komplexen mit Olefnen, VI. Reaktionen von Tricarbonyl-η5-2,4-cyclohexadienyl-mangan mit konjugierten Dienen / Photochemical Reactions of Transition Metal Organyl Complexes with Olefins, VI. Reactions of Tricarbonyl (η5-2,4-cyclohexadienyl)manganese with Conjugated Dienes". Zeitschrift für Naturforschung B 46, № 10 (1991): 1377–83. http://dx.doi.org/10.1515/znb-1991-1016.

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Tricarbonyl-η5-2,4-cyclohexadien-1-yl-manganese (1) was reacted photochemically at 253 K with simple conjugated dienes. Four different types of products were obtained, depending upon the dienes. With 1,3-butadiene (A) dicarbonyl-η4:3-1-(3-buten-1,2-diyl)-2,4-cyclohexadiene-manganese (2A) is isolated. 2-Methyl-1,3-butadiene (B) yields the methyl-substituted diastereomeric dicarbonyls 2B, 2B′, the [4+5]-cycloadduct tricarbonyl-η3:2-3-methyl-bicyclo-[4.3.1]-3,8-decadien-7-yl-manganese (3B) and tetracarbonyl-η3-4-methylene-bicyclo[4.3.1]-8-decen-3-yl-manganese (4B) with an exocyclically coordinate
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Huters, Alexander D., Evan D. Styduhar, and Neil K. Garg. "Total Syntheses of the Elusive Welwitindolinones with Bicyclo[4.3.1] Cores." Angewandte Chemie International Edition 51, no. 16 (2012): 3758–65. http://dx.doi.org/10.1002/anie.201107567.

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7

MOMOSE, Takefumi, Kikuo MASUDA, Sachiko FURUSAWA, Osamu MURAOKA, and Toshiyuki ITOOKA. "Bicyclo(3.3.1)nonanes as synthetic intermediates. XVII. A novel interconversion between bicyclo(4.3.1)decane and tricyclo(4.3.1.0)decane systems via the dual mode of aldol cyclization of bicyclo(4.3.1)decane-3,8-dione." CHEMICAL & PHARMACEUTICAL BULLETIN 38, no. 6 (1990): 1707–11. http://dx.doi.org/10.1248/cpb.38.1707.

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8

Trost, Barry M., Patrick J. McDougall, Olaf Hartmann, and Peter T. Wathen. "Asymmetric Synthesis of Bicyclo[4.3.1]decadienes and Bicyclo[3.3.2]decadienes via [6 + 3] Trimethylenemethane Cycloaddition with Tropones." Journal of the American Chemical Society 130, no. 45 (2008): 14960–61. http://dx.doi.org/10.1021/ja806979b.

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9

Srikrishna, A., C. Dinesh, and K. Anebouselvy. "Synthesis of chiral bicyclo[4.3.1]decanes via an intramolecular carbonyl ene-reaction." Tetrahedron Letters 40, no. 5 (1999): 1031–34. http://dx.doi.org/10.1016/s0040-4039(98)02518-0.

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10

Huters, Alexander D., Evan D. Styduhar, and Neil K. Garg. "ChemInform Abstract: Total Syntheses of the Elusive Welwitindolinones with Bicyclo[4.3.1] Cores." ChemInform 43, no. 34 (2012): no. http://dx.doi.org/10.1002/chin.201234204.

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Dissertations / Theses on the topic "Bicyclo[4.3.1]decanone"

1

Muscroft-Taylor, Andrew Clive. "Investigations of the type ii intramolecular Diels-Alder reaction directed toward natural product synthesis." Thesis, University of Canterbury. Chemistry, 2006. http://hdl.handle.net/10092/1290.

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This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and florlide marine natural products. Chapter One provides an overview of the importance of natural products to current medicinal chemistry and describes how the "supply issue" associated with these biologically derived compounds can be resolved through the process of total synthesis. Two families of marine natural products, the nakafurans and the florlides, are introduced as synthetic targets and strategies utilising a type II intramolecular Diels-Alder (IMDA) reaction to achieve their total synthesi
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