Synthesis and crystal structure analysis of substituted bicyclo[3.3.1]nonanones

A set of novel bi-cyclo-[3.3.1]nona-nones, namely, 4-methoxybi-cyclo-[3.3.1]non-3-ene-2,9-dione, C<sub>10</sub>H<sub>12</sub>O<sub>3</sub> (<b>1</b>), 4,9,9-tri-methoxybi-cyclo-[3.3.1]non-3-en-2-ol, C<sub>12</sub>H<sub>20</sub>O<sub>4</sub> (<b>2</b>), 4-meth-oxy-6-methyl-1-(3-methyl-but-2-en-1-yl)-6-(4-methyl-pent-3-en-1-yl)bi-cyclo-[3.3.1]non-3-ene-2,9-dione, C<sub>22</sub>H<sub>32</sub>O<sub>3</sub> (<b>3</b>) and 4-(<i>tert</i>-but-yl)-4-hy-droxy-2-meth-oxy-8-methyl-7-(3-methyl-but-2-en-1-yl)-8-(4-methyl-pent-3-en-1-yl)bi-cyclo-[3.3.1]non-2-en-9-one, C<sub>26</sub>H<sub>42</sub>O<sub>3</sub> (<b>4</b>), were synthesized and structurally elucidated by NMR, HRMS and X-ray crystallography.

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Publication Details

Journal
Acta Crystallographica Section E Crystallographic Communications
Published
2025-04-14
DOI
https://doi.org/10.1107/s2056989025003299
Primary Topic
Molecular spectroscopy and chirality
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis and crystal structure analysis of substituted bicyclo[3.3.1]nonanones

Julien A. König, Bernd Morgenstern, Johann Jauch
Acta Crystallographica Section E Crystallographic Communications
Molecular spectroscopy and chirality
article

Synthesis and crystal structure analysis of substituted bicyclo[3.3.1]nonanones

Julien A. König, Bernd Morgenstern, Johann Jauch
article en

Abstract

A set of novel bi-cyclo-[3.3.1]nona-nones, namely, 4-methoxybi-cyclo-[3.3.1]non-3-ene-2,9-dione, C<sub>10</sub>H<sub>12</sub>O<sub>3</sub> (<b>1</b>), 4,9,9-tri-methoxybi-cyclo-[3.3.1]non-3-en-2-ol, C<sub>12</sub>H<sub>20</sub>O<sub>4</sub> (<b>2</b>), 4-meth-oxy-6-methyl-1-(3-methyl-but-2-en-1-yl)-6-(4-methyl-pent-3-en-1-yl)bi-cyclo-[3.3.1]non-3-ene-2,9-dione, C<sub>22</sub>H<sub>32</sub>O<sub>3</sub> (<b>3</b>) and 4-(<i>tert</i>-but-yl)-4-hy-droxy-2-meth-oxy-8-methyl-7-(3-methyl-but-2-en-1-yl)-8-(4-methyl-pent-3-en-1-yl)bi-cyclo-[3.3.1]non-2-en-9-one, C<sub>26</sub>H<sub>42</sub>O<sub>3</sub> (<b>4</b>), were synthesized and structurally elucidated by NMR, HRMS and X-ray crystallography.

Acta Crystallographica Section E Crystallographic CommunicationsVol. 81(5)
Saarland University (DE)
Deutsche Forschungsgemeinschaft, Universität des Saarlandes
Openalex Percentile: Top 93%
Molecular spectroscopy and chirality
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