Literature DB >> 15065285

Three-component sequential aza[4+2] cycloaddition/allylboration/retro-sulfinyl-ene reaction: a new stereocontrolled entry to palustrine alkaloids and other 2,6-disubstituted piperidines.

Barry B Touré1, Dennis G Hall.   

Abstract

Entities:  

Year:  2004        PMID： 15065285     DOI： 10.1002/anie.200353152

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


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  3 in total

1.  Application of the aza-Achmatowicz oxidative rearrangement for the stereoselective synthesis of the Cassia and Prosopis alkaloid family.

Authors:  Carolyn A Leverett; Michael P Cassidy; Albert Padwa
Journal:  J Org Chem       Date:  2006-10-27       Impact factor: 4.354

Review 2.  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.  Stereoselective Allylic Alkylations of Amino Ketones and Their Application in the Synthesis of Highly Functionalized Piperidines.

Authors:  Cynthia Prudel; Kai Huwig; Uli Kazmaier
Journal:  Chemistry       Date:  2020-02-21       Impact factor: 5.236
  3 in total

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