Literature DB >> 17851618

A novel cyclization reaction between 2,3-bis(trimethylsilyl)buta-1,3-diene and acyl chlorides with straightforward formation of polysubstituted furans.

Francesco Babudri1, Stefania R Cicco, Gianluca M Farinola, Linda C Lopez, Francesco Naso, Vita Pinto.   

Abstract

A novel cyclization process of 2,3-bis(trimethylsilyl)buta-1,3-diene with various acyl chlorides in the presence of aluminium trichloride affords 2,5-disubstituted or 2,3,5-trisubstituted furans in short reaction time; a subsequent acylation process of the furan ring occurs if the reaction time is prolonged.

Entities:  

Year:  2007        PMID: 17851618     DOI: 10.1039/b705257j

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


  2 in total

1.  Highly substituted lactone/ester-containing furan library by the palladium-catalyzed carbonylation of hydroxyl-substituted 3-iodofurans.

Authors:  Chul-Hee Cho; Richard C Larock
Journal:  ACS Comb Sci       Date:  2011-03-24       Impact factor: 3.784

2.  Multicomponent type II anion relay chemistry (ARC): one-pot syntheses of 2,3-disubstituted furans and thiophenes.

Authors:  Nelmi O Devarie-Baez; Won-Suk Kim; Amos B Smith; Ming Xian
Journal:  Org Lett       Date:  2009-04-16       Impact factor: 6.005

  2 in total

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