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Cycloadditions of isobenzofuran to a constrained template bearing neighboring dienophiles
journal contribution
posted on 2017-12-06, 00:00 authored by M Stoermer, Douglas ButlerDouglas Butler, Ronald WarrenerRonald Warrener, K Weerasuria, D FairlieA 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.
Funding
Category 1 - Australian Competitive Grants (this includes ARC, NHMRC)
History
Volume
9Issue
9Start Page
2068End Page
2071Number of Pages
4ISSN
0947-6539Location
GermanyPublisher
Wiley-VCH Verlag GMBHPublisher DOI
Full Text URL
Language
en-ausPeer Reviewed
- Yes
Open Access
- No
Era Eligible
- Yes
