Literature DB >> 15834484

An iron-catalysed chemo- and regioselective tetrahydrofuran synthesis.

Gerhard Hilt1, Patrick Bolze, Iris Kieltsch.   

Abstract

An intermolecular ring expansion reaction of an aryl epoxide with several dienes, acrylates, enynes or styrenes under iron catalysis, generated tetrahydrofuran derivatives in a highly chemo- and regioselective fashion. The process could be used in an unprecedented way for the one step synthesis of racemic calyxolane A and calyxolane B with acceptable diastereoselectivity.

Entities:  

Year:  2005        PMID: 15834484     DOI: 10.1039/b501100k

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


  2 in total

1.  Activation and discovery of earth-abundant metal catalysts using sodium tert-butoxide.

Authors:  Jamie H Docherty; Jingying Peng; Andrew P Dominey; Stephen P Thomas
Journal:  Nat Chem       Date:  2017-01-09       Impact factor: 24.427

2.  HFIP-Promoted Synthesis of Substituted Tetrahydrofurans by Reaction of Epoxides with Electron-Rich Alkenes.

Authors:  Natalia Llopis; Alejandro Baeza
Journal:  Molecules       Date:  2020-07-30       Impact factor: 4.411

  2 in total

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