anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-diene
The title compound, C22H20Cl8O4, was prepared as part of the synthesis of precursors for the preparation of fluorinated molecular tweezers. The molecule sits on an inversion center, thus requiring that the cyclooctane ring adopt a chair conformation.
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
International Union of Crystallography
2010-08-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536810024669 |
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author | Megan E. Tenbusch Matthew D. Brooker Jacob C. Timmerman Daniel S. Jones Markus Etzkorn |
author_facet | Megan E. Tenbusch Matthew D. Brooker Jacob C. Timmerman Daniel S. Jones Markus Etzkorn |
author_sort | Megan E. Tenbusch |
collection | DOAJ |
description | The title compound, C22H20Cl8O4, was prepared as part of the synthesis of precursors for the preparation of fluorinated molecular tweezers. The molecule sits on an inversion center, thus requiring that the cyclooctane ring adopt a chair conformation. |
first_indexed | 2024-12-13T00:38:06Z |
format | Article |
id | doaj.art-d246ef92d08b405496c5d6fd7699d87f |
institution | Directory Open Access Journal |
issn | 1600-5368 |
language | English |
last_indexed | 2024-12-13T00:38:06Z |
publishDate | 2010-08-01 |
publisher | International Union of Crystallography |
record_format | Article |
series | Acta Crystallographica Section E |
spelling | doaj.art-d246ef92d08b405496c5d6fd7699d87f2022-12-22T00:05:11ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-08-01668o1882o188210.1107/S1600536810024669anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-dieneMegan E. TenbuschMatthew D. BrookerJacob C. TimmermanDaniel S. JonesMarkus EtzkornThe title compound, C22H20Cl8O4, was prepared as part of the synthesis of precursors for the preparation of fluorinated molecular tweezers. The molecule sits on an inversion center, thus requiring that the cyclooctane ring adopt a chair conformation.http://scripts.iucr.org/cgi-bin/paper?S1600536810024669 |
spellingShingle | Megan E. Tenbusch Matthew D. Brooker Jacob C. Timmerman Daniel S. Jones Markus Etzkorn anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-diene Acta Crystallographica Section E |
title | anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-diene |
title_full | anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-diene |
title_fullStr | anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-diene |
title_full_unstemmed | anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-diene |
title_short | anti-1′,6′,7′,8′,9′,14′,15′,16′-Octachlorodispiro[1,3-dioxolane-2,17′-pentacyclo[12.2.1.16,9.02,13.05,10]octadecane-18′,2′′-1,3-dioxolane]-7′,15′-diene |
title_sort | anti 1 amp 8242 6 amp 8242 7 amp 8242 8 amp 8242 9 amp 8242 14 amp 8242 15 amp 8242 16 amp 8242 octachlorodispiro 1 3 dioxolane 2 17 amp 8242 pentacyclo 12 2 1 16 9 02 13 05 10 octadecane 18 amp 8242 2 amp 8242 amp 8242 1 3 dioxolane 7 amp 8242 15 amp 8242 diene |
url | http://scripts.iucr.org/cgi-bin/paper?S1600536810024669 |
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