Relevant bibliographies by topics / Bicyclo[3.3.1]nonane

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  1. Journal articles

Academic literature on the topic 'Bicyclo[3.3.1]nonane'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Bicyclo[3.3.1]nonane"

1

Brunelli, Michela, Marcus A. Neumann, Andrew N. Fitch, and Asiloé J. Mora. "Temperature phase changes in solid bicyclo[3.3.1]nonane-2,6-dione and bicyclo[3.3.1]nonane-3,7-dione from powder X-ray diffraction data." Journal of Applied Crystallography 40, no. 4 (2007): 702–9. http://dx.doi.org/10.1107/s0021889807028087.

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The crystal structures of bicyclo[3.3.1]nonane-2,6-dione and bicyclo[3.3.1]nonane-3,7-dione have been solved by direct methods and by direct-space simulated annealing, respectively, from powder synchrotron X-ray diffraction data. Both compounds have a transition to a face-centred-cubic orientationally disordered phase (phase I) near 363 K, as shown by differential scanning calorimetry and powder diffraction measurements. Phase II of bicyclo[3.3.1]nonane-2,6-dione, which occurs below 363 K, is monoclinic, space groupC2/c, witha= 7.38042 (4),b= 10.38220 (5),c= 9.75092 (5) Å and β = 95.359 (1)° a
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2

Zhu, Hui, Ya-Nan Yang, Kuo Xu, et al. "Sophopterocarpan A, a novel pterocarpine derivative with a benzotetrahydrofuran-fused bicyclo [3.3.1] nonane from Sophora flavescens." Organic & Biomolecular Chemistry 15, no. 26 (2017): 5480–83. http://dx.doi.org/10.1039/c7ob01261f.

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3

Zaytsev, Andrey V., James E. Pickles, Suzannah J. Harnor, et al. "Concise syntheses of bridged morpholines." RSC Advances 6, no. 59 (2016): 53955–57. http://dx.doi.org/10.1039/c6ra08737j.

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Practical syntheses of 8-oxa-3-aza-bicyclo[3.2.1]octane and 9-oxa-3-aza-bicyclo[3.3.1]nonane, useful intermediates for synthesising kinase inhibitors, were achieved from readily available starting materials, using a solvent-free thermolytic cyclisation for the key step.
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4

Laszlo, Ilona. "The conformation of bicyclo[3.3.1]nonane." Recueil des Travaux Chimiques des Pays-Bas 84, no. 2 (2010): 251–54. http://dx.doi.org/10.1002/recl.19650840213.

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5

Bagdžiūnas, Gintautas, Sigitas Stončius, and Eugenijus Butkus. "Synthesis of Star-Shaped Aromatic Derivatives with Chirality Predetermined by Bicyclo[3.3.1]nonane Framework." Synlett 28, no. 20 (2017): 2790–94. http://dx.doi.org/10.1055/s-0036-1590833.

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Star-shaped aromatic derivatives of bicyclo[3.3.1]nonane with predetermined chirality were synthesized by employing the Suzuki and Sonogashira reactions. The C 3-symmetric trifunctional aromatic derivatives based on the lateral bicyclo[3.3.1]nonene moiety possess unique molecular structures. The chiroptical properties of the star-shaped compounds and the corresponding monomeric derivatives were studied, and the absolute configuration was confirmed by using the empirical octant rule for the carbonyl chromophore and the sector rule for the aromatic chromophore.
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6

Tian, Wen-Jing, Yu-Qin Qiu, Xiao-Jie Jin, et al. "Hypersampsones S–W, new polycyclic polyprenylated acylphloroglucinols from Hypericum sampsonii." RSC Advances 6, no. 56 (2016): 50887–94. http://dx.doi.org/10.1039/c5ra26332h.

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7

Ren, Xiaoli, Yifei Ling, and Jun Luo. "Synthesis of Bicyclo[3.3.1]nonane-2,6,9-trione." Chinese Journal of Organic Chemistry 34, no. 2 (2014): 376. http://dx.doi.org/10.6023/cjoc201309009.

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8

MacCorquodale, Finlay, and John C. Walton. "Formation of bicyclo[3.2.1]octane, bicyclo[4.2.1]nonane, and bicyclo[3.3.1]nonane by transannular radical cyclisations." Journal of the Chemical Society, Chemical Communications, no. 19 (1987): 1456. http://dx.doi.org/10.1039/c39870001456.

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9

Butkus, Eugenius, Arvydas Stoncius, Jule Malinauskiene, Shuji Tomoda, and Daisuke Kaneno. "Stereoelectronic and conformational effects on the stereochemical course of reduction of bicyclo[3.3.1]nonane 1,3-diketones." Canadian Journal of Chemistry 79, no. 11 (2001): 1598–605. http://dx.doi.org/10.1139/v01-131.

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The stereoselectivity of the reduction of bicyclo[3.3.1]nonane 1,3-diketones was studied. The experimental data of π-facial stereoselection of the reduction of the carbonyl group were successfully rationalized by the application of the exterior frontier orbital extension (EFOE) model. The observed facial diastereoselectivity of the carbonyl reduction of bicyclo[3.3.1]nonane diketones could be reasonably explained by the ground-state facial anisotropy of the frontier orbital extension, steric effects, and the intrinsic reactivity of carbonyl groups. Although the EFOE density and PDAS values pre
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10

Yang, Jae-Deuk, Moon-Soo Kim, Miai Lee, Woonphil Baik, and Sangho Koo. "Highly Efficient Synthesis of Bicyclo[3.3.1]nonane Skeleton." Synthesis 2000, no. 06 (2000): 801–4. http://dx.doi.org/10.1055/s-2000-6275.

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