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.

Bibliographic Details
Main Authors: Megan E. Tenbusch, Matthew D. Brooker, Jacob C. Timmerman, Daniel S. Jones, Markus Etzkorn
Format: Article
Language:English
Published: International Union of Crystallography 2010-08-01
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.
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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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