Literature DB >> 20000615

Practical synthesis and reactivity of [3]dendralene.

Tanya A Bradford1, Alan D Payne, Anthony C Willis, Michael N Paddon-Row, Michael S Sherburn.   

Abstract

A convenient and high-yielding three-step synthesis of the simplest branched triene, [3]dendralene, has been devised. The synthesis is robust and operationally simple, requiring no chromatography and involving no protecting groups or specialized equipment, allowing the synthesis of the volatile hydrocarbon in pure, solvent free form on a multigram scale. The stability, dimerization when stored neat, and Diels-Alder reactivity of [3]dendralene--including double cycloaddition sequences and catalytic enantioselective variant--are reported.

Entities:  

Year:  2010        PMID: 20000615     DOI: 10.1021/jo9024557

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Synthesis of cross-conjugated trienes by rhodium-catalyzed dimerization of monosubstituted allenes.

Authors:  Tomoya Miura; Tsuneaki Biyajima; Takeharu Toyoshima; Masahiro Murakami
Journal:  Beilstein J Org Chem       Date:  2011-05-09       Impact factor: 2.883

2.  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 in total

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