Octacyclopropylcubane and Some of Its Isomers
Decorator rocket fuel? Tricyclooctadiene 1, easily prepared in a single‐pot operation from dicyclopropylethyne in 67 % yield, upon irradiation in pentane solution undergoes an intramolecular [2+2] cycloaddition to give octacyclopropylcubane (2) in remarkably good yield (48 %). The new cubane derivat...
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Veröffentlicht in: | Angewandte Chemie International Edition 2007-06, Vol.46 (24), p.4574-4576 |
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creator | de Meijere, Armin Redlich, Stefan Frank, Daniel Magull, Jörg Hofmeister, Anja Menzel, Henning König, Burkhard Svoboda, Jiri |
description | Decorator rocket fuel? Tricyclooctadiene 1, easily prepared in a single‐pot operation from dicyclopropylethyne in 67 % yield, upon irradiation in pentane solution undergoes an intramolecular [2+2] cycloaddition to give octacyclopropylcubane (2) in remarkably good yield (48 %). The new cubane derivative with an overall strain energy of >390 kcal mol−1 displays unique physical and chemical properties. |
doi_str_mv | 10.1002/anie.200605150 |
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Tricyclooctadiene 1, easily prepared in a single‐pot operation from dicyclopropylethyne in 67 % yield, upon irradiation in pentane solution undergoes an intramolecular [2+2] cycloaddition to give octacyclopropylcubane (2) in remarkably good yield (48 %). The new cubane derivative with an overall strain energy of >390 kcal mol−1 displays unique physical and chemical properties.</description><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.200605150</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag</publisher><subject>cage compounds ; cyclopropanes ; photochemistry ; strained molecules ; thermal isomerization</subject><ispartof>Angewandte Chemie International Edition, 2007-06, Vol.46 (24), p.4574-4576</ispartof><rights>Copyright © 2007 WILEY‐VCH Verlag GmbH & Co. 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Tricyclooctadiene 1, easily prepared in a single‐pot operation from dicyclopropylethyne in 67 % yield, upon irradiation in pentane solution undergoes an intramolecular [2+2] cycloaddition to give octacyclopropylcubane (2) in remarkably good yield (48 %). 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Tricyclooctadiene 1, easily prepared in a single‐pot operation from dicyclopropylethyne in 67 % yield, upon irradiation in pentane solution undergoes an intramolecular [2+2] cycloaddition to give octacyclopropylcubane (2) in remarkably good yield (48 %). The new cubane derivative with an overall strain energy of >390 kcal mol−1 displays unique physical and chemical properties.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag</pub><doi>10.1002/anie.200605150</doi><tpages>3</tpages></addata></record> |
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subjects | cage compounds cyclopropanes photochemistry strained molecules thermal isomerization |
title | Octacyclopropylcubane and Some of Its Isomers |
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