Literature DB >> 15646970

A two-step reaction sequence for the syntheses of tetrahydronaphthalenes.

Gerhard Hilt1, Steffen Lüers, Konstantin I Smolko.   

Abstract

[Reaction: see text] A cobalt(I)-catalyzed Diels-Alder reaction of a boron-functionalized enyne is the key step in a two-step reaction cascade interconnecting four simple starting materials to obtain polycyclic multifunctionalized products in good yields and with a very high degree of diastereoselectivity.

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Year:  2005        PMID: 15646970     DOI: 10.1021/ol0477879

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


  2 in total

Review 1.  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

2.  Iridium-catalyzed intramolecular [4 + 2] cycloadditions of alkynyl halides.

Authors:  Andrew Tigchelaar; William Tam
Journal:  Beilstein J Org Chem       Date:  2012-10-16       Impact factor: 2.883

  2 in total

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