Literature DB >> 23148030

Dienamine-mediated inverse-electron-demand hetero-diels-alder reaction by using an enantioselective H-bond-directing strategy.

Lukasz Albrecht1, Gustav Dickmeiss, Christian F Weise, Carles Rodríguez-Escrich, Karl Anker Jørgensen.   

Abstract

Giving directions: optically active dihydropyrans bearing three contiguous stereogenic centers can be efficiently prepared by the title reaction. High stereo- and regiocontrol can be achieved by employing a bifunctional H-bond-directing aminocatalyst.
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2012        PMID: 23148030     DOI: 10.1002/anie.201207122

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  3 in total

1.  An Asymmetric Vinylogous Michael Cascade of Silyl Glyoximide, Vinyl Grignard, and Nitroalkenes via Long Range Stereoinduction.

Authors:  Gregory R Boyce; Jeffrey S Johnson
Journal:  J Org Chem       Date:  2016-02-02       Impact factor: 4.354

2.  Old tricks, new dogs: organocatalytic dienamine activation of α,β-unsaturated aldehydes.

Authors:  Vanesa Marcos; José Alemán
Journal:  Chem Soc Rev       Date:  2016-11-02       Impact factor: 54.564

Review 3.  Recent Advances in Inverse-Electron-Demand Hetero-Diels-Alder Reactions of 1-Oxa-1,3-Butadienes.

Authors:  Aleksandra Pałasz
Journal:  Top Curr Chem (Cham)       Date:  2016-04-20
  3 in total

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