Cycloadditions of isobenzofuran to a constrained template bearing neighboring dienophiles
| Contribuinte(s) |
Willie E E |
|---|---|
| Data(s) |
01/01/2003
|
| Resumo |
A high yielding synthesis of the pentacyclic diene-dione 1 has enabled investigation of its reactivity as a double dienophile in Diels-Alder [4+2] cycloadditions with isobenzofuran, leading to novel and highly symmetrical three-sided cavitands 3 and 4. |
| Identificador | |
| Idioma(s) |
eng |
| Publicador |
Wiley - V C H Verlag GmbH & Co. KGaA |
| Palavras-Chave | #Chemistry, Multidisciplinary #Cavitands #Cycloaddition #Nmr Spectroscopy #Semiempirical Calculations #Supramolecular Chemistry #Diels-alder Reactions #Cyclopentadiene #Construction #Systems #CX #250301 Organic Chemical Synthesis #780103 Chemical sciences |
| Tipo |
Journal Article |
