Literature DB >> 10956538

Stereoselective diels-alder reactions of chiral anthracenes

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Abstract

Various chiral (9-anthryl)carbinol templates undergo Diels-Alder cycloadditions with a variety of symmetric and nonsymmetric dienophiles with excellent pi-facial selectivity and regioselectivity, under both thermal and Lewis acid catalyzed conditions.

Entities:  

Year:  2000        PMID： 10956538     DOI： 10.1021/ol006206m

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


  3 in total

1.  Enantioselective syntheses of candenatenins B and C using a chiral anthracene auxiliary.

Authors:  Amanda L Jones; Xiang Liu; John K Snyder
Journal:  Tetrahedron Lett       Date:  2010-02-17       Impact factor: 2.415

2.  Intramolecular rhodium-catalyzed [2+2+2] cyclizations of diynes with enones.

Authors:  Amanda L Jones; John K Snyder
Journal:  J Org Chem       Date:  2009-04-03       Impact factor: 4.354

3.  Diels-Alder Reactivity of a Chiral Anthracene Template with Symmetrical and Unsymmetrical Dienophiles: A DFT Study.

Authors:  Jennifer P Hernández-Mancera; Francisco Núñez-Zarur; Ricardo Vivas-Reyes
Journal:  ChemistryOpen       Date:  2020-07-10       Impact factor: 2.911
  3 in total

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