Literature DB >> 21077631

Friedel-Crafts acylation of pyrroles and indoles using 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) as a nucleophilic catalyst.

James E Taylor1, Matthew D Jones, Jonathan M J Williams, Steven D Bull.   

Abstract

1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) has been shown to be an effective catalyst for the regioselective Friedel-Crafts C-acylation of pyrroles and indoles in high yields. A detailed mechanistic study implies that DBN is acting as a nucleophilic organocatalyst, with the X-ray crystal structure of a key N-acyl-amidine intermediate having been determined for the first time.

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Year:  2010        PMID: 21077631     DOI: 10.1021/ol1025348

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


  4 in total

1.  Application of a robustness screen for the evaluation of synthetic organic methodology.

Authors:  Karl D Collins; Andreas Rühling; Frank Glorius
Journal:  Nat Protoc       Date:  2014-05-15       Impact factor: 13.491

2.  2,2-Dichloro-1-(3,3,6-trimethyl-9-oxo-1,5-diaza-bicyclo-[4.3.0]nonan-5-yl)ethanone.

Authors:  Ying Fu; Fei Ye
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-07-13

3.  The fast and efficient KI/H2O2 mediated 2-sulfonylation of indoles and N-methylpyrrole in water.

Authors:  Jun Zhang; Zhong Wang; Lingjuan Chen; Yan Liu; Ping Liu; Bin Dai
Journal:  RSC Adv       Date:  2018-12-12       Impact factor: 4.036

4.  Isothiourea-catalysed enantioselective pyrrolizine synthesis: synthetic and computational studies.

Authors:  Daniel G Stark; Patrick Williamson; Emma R Gayner; Stefania F Musolino; Ryan W F Kerr; James E Taylor; Alexandra M Z Slawin; Timothy J C O'Riordan; Stuart A Macgregor; Andrew D Smith
Journal:  Org Biomol Chem       Date:  2016-08-04       Impact factor: 3.876

  4 in total

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