Literature DB >> 18302410

From furans to anilines: toward one-pot two-step amination/diels-alder sequences.

Raouf Medimagh1, Sylvain Marque, Damien Prim, Saber Chatti, Hédi Zarrouk.   

Abstract

Selective metal-free amination and Diels-Alder reactions are described in the furan series, leading to polysubstituted anilines or to stable oxabicyclic adducts in high yield. Interestingly, anilines are conveniently prepared through a novel one-pot, two-step amination/Diels-Alder procedure from commercially available 5-bromo-2-furaldehyde.

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Year:  2008        PMID: 18302410     DOI: 10.1021/jo7024916

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


  3 in total

1.  Pyridazine N-Oxides as Precursors to 2-Aminofurans: Scope and Limitations in Complexity Building Cascade Reactions.

Authors:  Maribel Borger; James H Frederich
Journal:  Org Lett       Date:  2019-03-22       Impact factor: 6.072

Review 2.  The Interplay between Kinetics and Thermodynamics in Furan Diels-Alder Chemistry for Sustainable Chemicals Production.

Authors:  Răzvan C Cioc; Marc Crockatt; Jan C van der Waal; Pieter C A Bruijnincx
Journal:  Angew Chem Int Ed Engl       Date:  2022-02-10       Impact factor: 16.823

3.  (3aR,6S,7aR)-7a-Chloro-2-[(4-nitro-phen-yl)sulfon-yl]-1,2,3,6,7,7a-hexa-hydro-3a,6-ep-oxy-iso-indole.

Authors:  Ersin Temel; Aydın Demircan; Muhammet Kasım Kandemir; Medine Colak; Orhan Büyükgüngör
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-09-18
  3 in total

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