Literature DB >> 16131173

Practical synthesis and Diels-Alder chemistry of [4]dendralene.

Alan D Payne1, Anthony C Willis, Michael S Sherburn.   

Abstract

Spectacular new atom efficient domino cycloaddition sequences involving [4]dendralene, the simplest cross-conjugated tetraene, are reported. Up to eight stereocenters, three new rings, and six C-C bonds are generated in one synthetic operation. The site selectivity of dienophile addition to cross-conjugated trienes and tetraenes is controlled with a simple Lewis acid.

Entities:  

Year:  2005        PMID： 16131173     DOI： 10.1021/ja053772+

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


  2 in total

1.  Fluorescent hexaaryl- and hexa-heteroaryl[3]radialenes: Synthesis, structures, and properties.

Authors:  Antonio Avellaneda; Courtney A Hollis; Xin He; Christopher J Sumby
Journal:  Beilstein J Org Chem       Date:  2012-01-11       Impact factor: 2.883

2.  Controlling the conformational changes in donor-acceptor [4]-dendralenes through intramolecular charge-transfer processes.

Authors:  Alexander L Kanibolotsky; John C Forgie; Greg J McEntee; M Munsif A Talpur; Peter J Skabara; Thomas D J Westgate; Joseph J W McDouall; Michael Auinger; Simon J Coles; Michael B Hursthouse
Journal:  Chemistry       Date:  2009-11-02       Impact factor: 5.236
  2 in total

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