Literature DB >> 16597104

Regioselective dicouplings: application to differentially substituted pyrroles.

Scott T Handy1, Jesse J Sabatini.   

Abstract

[reaction: see text] In an effort to develop a more concise route to differentially substituted pyrroles (such as that found in the lamellarins), a completely regioselective one-pot double Suzuki coupling has been discovered. The key feature is the use of a ligand-free palladium catalyst under optimized conditions, which results only in coupling of the C5 bromide. At this point, addition of a second boronic acid and a phosphine ligand enables coupling at the remaining C4 bromide.

Entities:  

Year:  2006        PMID: 16597104     DOI: 10.1021/ol0530981

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  5 in total

1.  Regioselective double Suzuki couplings of 4,5-dibromothiophene-2-carboxaldehyde.

Authors:  Scott T Handy; Diyar Mayi
Journal:  Tetrahedron Lett       Date:  2007-11-12       Impact factor: 2.415

2.  Studies of one-pot double couplings on dibromoquinolines.

Authors:  Alexander Piala; Diyar Mayi; Scott T Handy
Journal:  Tetrahedron       Date:  2011-06-10       Impact factor: 2.457

3.  One-pot Double Suzuki Couplings of Dichloropyrimidines.

Authors:  Samantha C Anderson; Scott T Handy
Journal:  Synthesis (Stuttg)       Date:  2010-08-01       Impact factor: 3.157

4.  Double Couplings of Dibromothiophenes using Boronic Acids and Boronates.

Authors:  Samantha Varello; Scott T Handy
Journal:  Synthesis (Stuttg)       Date:  2009-05-12       Impact factor: 3.157

Review 5.  Lamellarins and related pyrrole-derived alkaloids from marine organisms.

Authors:  Hui Fan; Jiangnan Peng; Mark T Hamann; Jin-Feng Hu
Journal:  Chem Rev       Date:  2007-12-21       Impact factor: 60.622

  5 in total

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