Literature DB >> 16292385

Highly efficient [2 + 2] intramolecular cyclizations of allenynes under microwave irradiation: construction of fused bicyclic compounds.

Chang Ho Oh1, Arun Kumar Gupta, Dai In Park, Nakjoong Kim.   

Abstract

A palladium [2 + 2] cycloaddition of 1,6- and 1,7-allenyne carboxylates and microwave-mediated [2 + 2] cycloaddition of various 1,n-allenynes were developed and, particularly, the microwave irradiated [2 + 2] cycloaddition of allenynes can provide a simple, general and eco-friendly synthetic method to fused bicyclo[m,2,0]alkadienes.

Entities:  

Year:  2005        PMID: 16292385     DOI: 10.1039/b508306k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Gold-catalyzed cycloisomerization of 1,5-allenynes via dual activation of an ene reaction.

Authors:  Paul Ha-Yeon Cheong; Philip Morganelli; Michael R Luzung; K N Houk; F Dean Toste
Journal:  J Am Chem Soc       Date:  2008-03-08       Impact factor: 15.419

2.  Intramolecular thermal allenyne [2 + 2] cycloadditions; facile construction of the 5-6-4 ring core of sterpurene.

Authors:  Timo V Ovaska; Robert E Kyne
Journal:  Tetrahedron Lett       Date:  2008-01-07       Impact factor: 2.415

3.  A thermally-induced, tandem [3,3]-sigmatropic rearrangement/[2 + 2] cycloaddition approach to carbocyclic spirooxindoles.

Authors:  Kay M Brummond; Joshua M Osbourn
Journal:  Beilstein J Org Chem       Date:  2010-04-08       Impact factor: 2.883

  3 in total

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