Literature DB >> 12740855

Cycloadditions of isobenzofuran to a constrained template bearing neighboring dienophiles.

Martin J Stoermer1, Douglas N Butler, Ronald N Warrener, K D V Weerasuria, David P Fairlie.   

Abstract

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.

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Year:  2003        PMID： 12740855     DOI： 10.1002/chem.200204619

Source DB:  PubMed          Journal:  Chemistry        ISSN： 0947-6539            Impact factor:   5.236


  1 in total

1.  Synthesis and biological evaluation of rigid polycyclic derivatives of the Diels-Alder adduct tricyclo[6.2.1.02,7]undeca-4,9-dien-3,6-dione.

Authors:  Felicia Megumi Ito; Jacqueline Marques Petroni; Dênis Pires de Lima; Adilson Beatriz; Maria Rita Marques; Manoel Odorico de Moraes; Letícia Veras Costa-Lotufo; Raquel Carvalho Montenegro; Hemerson Iury Ferreira Magalhães; Cláudia do O Pessoa
Journal:  Molecules       Date:  2007-02-27       Impact factor: 4.411
  1 in total

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