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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 Butler, Ronald 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.

Funding

Category 1 - Australian Competitive Grants (this includes ARC, NHMRC)

History

Volume

9

Issue

9

Start Page

2068

End Page

2071

Number of Pages

4

ISSN

0947-6539

Location

Germany

Publisher

Wiley-VCH Verlag GMBH

Publisher DOI

Full Text URL

Language

en-aus

Peer Reviewed

  • Yes

Open Access

  • No

Era Eligible

  • Yes

Journal

Chemistry : a European journal.

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    Categories

    Keywords

    CavitandsCycloadditionNMR spectroscopySemiempirical calculationsSupramolecular chemistryChemical Sciences not elsewhere classified

    Licence

    CQUniversity General 1.0

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