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Cycloadditions of isobenzofuran to a constrained template bearing neighboring dienophiles
journal contributionposted on 2017-12-06, 00:00 authored by M Stoermer, Douglas ButlerDouglas Butler, Ronald WarrenerRonald Warrener, K Weerasuria, D Fairlie
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.
Category 1 - Australian Competitive Grants (this includes ARC, NHMRC)
Number of Pages4
PublisherWiley-VCH Verlag GMBH
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