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Controlled diastereoselectivity at the alkene-geometry through selective encapsulation: E-Z photoisomerization of oxazolidinone-functionalized enecarbamates within hydrophobic nano-cavities.
Saito, Hideaki; Sivaguru, J; Jockusch, Steffen; Dyer, Joanne; Inoue, Yoshihisa; Adam, Waldemar; Turro, Nicholas J.
Afiliação
  • Saito H; Department of Chemistry, Columbia University, 3000 Broadway, Mail Code 3119, New York, NY 10027, USA.
Chem Commun (Camb) ; (8): 819-21, 2007 Feb 28.
Article em En | MEDLINE | ID: mdl-17308642
ABSTRACT
Photoisomerization of encapsulated Z-enecarbamates within the hydrophobic chiral cavities of gamma-CD showed higher diastereoselectivities in the photoproducts than those obtained in solution. The selective encapsulation of the enecarbamates and the following isomerization process are both diastereoselectively controlled by gamma-CD.
Assuntos
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Bases de dados: MEDLINE Assunto principal: Carbamatos / Oxazolidinonas / Alcenos Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Bases de dados: MEDLINE Assunto principal: Carbamatos / Oxazolidinonas / Alcenos Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos