Literature DB >> 12585428

A novel diastereoselective route to alpha-hydroxyalkyl dihydropyrans using a hetero Diels-Alder/allylboration sequence.

Michael Deligny1, François Carreaux, Bertrand Carboni, Loïc Toupet, Gilles Dujardin.   

Abstract

The development of a new strategy for the synthesis of alpha-hydroxyalkyl dihydropyrans is reported. This approach is based on a tandem hetero[4+2]/allylboration reaction.

Entities:  

Year:  2003        PMID： 12585428

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


  3 in total

1.  Catalytic enantioselective diversity-oriented synthesis of a small library of polyhydroxylated pyrans inspired from thiomarinol antibiotics.

Authors:  Raed M Al-Zoubi; Dennis G Hall
Journal:  Mol Divers       Date:  2014-08-24       Impact factor: 2.943

Review 2.  Recent advances in the chemistry and biology of naturally occurring antibiotics.

Authors:  K C Nicolaou; Jason S Chen; David J Edmonds; Anthony A Estrada
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

Review 3.  Boron-substituted 1,3-dienes and heterodienes as key elements in multicomponent processes.

Authors:  Ludovic Eberlin; Fabien Tripoteau; François Carreaux; Andrew Whiting; Bertrand Carboni
Journal:  Beilstein J Org Chem       Date:  2014-01-22       Impact factor: 2.883
  3 in total

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