Generation and Reactions of an Octacyclic Hindered Pyramidalized Alkene

Octacyclo[10.6.1.01,10.03,7.04,9.08,19.011,16.013,17]-nonadeca-5,8,14-triene (27), a hindered pyramidalized alkene, has been generated from a diiodide precursor. Contrary to the usual behavior of known pyramidalized alkenes, no Diels−Alder adducts were obtained from the present alkene when it was ge...

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Detalhes bibliográficos
Autores: Camps García, Pelayo, Lozano Mena, David, Barbaraci, C., Font Bardia, Ma. Mercedes, Luque Garriga, F. Xavier, Estarellas, Carolina
Formato: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2018
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/161888
Acesso em linha:https://hdl.handle.net/2445/161888
Access Level:acceso abierto
Palavra-chave:Hidrocarburs
Oligòmers
Sílice
Mescles
Sodi
Hydrocarbons
Oligomers
Silica
Mixtures
Sodium
Descrição
Resumo:Octacyclo[10.6.1.01,10.03,7.04,9.08,19.011,16.013,17]-nonadeca-5,8,14-triene (27), a hindered pyramidalized alkene, has been generated from a diiodide precursor. Contrary to the usual behavior of known pyramidalized alkenes, no Diels−Alder adducts were obtained from the present alkene when it was generated by different standard procedures in the presence of different dienes. However, products derived from the reduction, t-BuLi addition, condensation with the solvent, or dimerization were isolated from these reactions, depending on the conditions used to generate it. No [2 + 2] cross product among this pyramidalized alkene and tricyclo[3.3.1.03,7]non-3(7)-ene was formed when a mixture of the corresponding precursor diiodides was reacted with sodium amalgam. The analysis of selected geometrical and orbital parameters determined from quantum mechanical calculations indicates that the degree of pyramidalization of this alkene and its higher steric hindrance compared with other polycyclic pyramidalized alkenes may explain its peculiar reactivity.