Literature DB >> 11073683

Tandem Aza

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Abstract

The alpha-hydroxyalkyl piperidine unit is common to several naturally occurring alkaloids and azasugar analogues. Polysubstituted piperidine derivatives of this kind (3), embodying four stereogenic centers, are formed in just a single operation from the highly stereocontrolled reaction of 4-borono-1-azadienes (1), maleimides, and aldehydes. This novel multicomponent reaction which affords as many as four elements of diversity should prove highly valuable in combinatorial chemistry and natural product synthesis.

Entities:  

Year:  2000        PMID: 11073683     DOI: 10.1021/ol006626b

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


  5 in total

1.  The catalytic asymmetric Diels-Alder reactions and post-cycloaddition reductive transpositions of 1-hydrazinodienes.

Authors:  Hao Xie; Glenn M Sammis; Eric M Flamme; Christina M Kraml; Erik J Sorensen
Journal:  Chemistry       Date:  2011-09-05       Impact factor: 5.236

2.  The synthesis of highly functionalised pyridines using Ghosez-type reactions of dihydropyrazoles.

Authors:  Federica Catti; Paula S Kiuru; Alexandra M Z Slawin; Nicholas J Westwood
Journal:  Tetrahedron       Date:  2008-09-29       Impact factor: 2.457

3.  Permuting Diels-Alder and Robinson Annulation Stereopatterns.

Authors:  Feng Peng; Mingji Dai; Angie R Angeles; Samuel J Danishefsky
Journal:  Chem Sci       Date:  2012-08-01       Impact factor: 9.825

Review 4.  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

Review 5.  Recent advances in the chemistry of imine-based multicomponent reactions (MCRs).

Authors:  Lokman H Choudhury; Tasneem Parvin
Journal:  Tetrahedron       Date:  2011-07-18       Impact factor: 2.457

  5 in total

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