Literature DB >> 17878964

Synthesis of azabicyclic systems using nitrogen-directed radical rearrangements.

David M Hodgson1, Leonard H Winning.   

Abstract

Radical rearrangements are important transformations in organic synthesis. The stabilisation of alpha-nitrogen radicals is shown to be a useful effect for the control of radical rearrangements and is applied to the synthesis of a variety of azabicyclic frameworks. The utility of this method is illustrated in the synthesis of bioactive targets.

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Year:  2007        PMID: 17878964     DOI: 10.1039/b707566a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

1.  A versatile enantioselective synthesis of azabicyclic ring systems: a concise total synthesis of (+)-grandisine D and unnatural analogues.

Authors:  Olugbeminiyi O Fadeyi; Timothy J Senter; Kristopher N Hahn; Craig W Lindsley
Journal:  Chemistry       Date:  2012-03-30       Impact factor: 5.236

2.  A General, Enantioselective Synthesis of 1-Azabicyclo[m.n.0]alkane Ring Systems.

Authors:  Timothy J Senter; Michael L Schulte; Leah C Konkol; Tyler E Wadzinski; Craig W Lindsley
Journal:  Tetrahedron Lett       Date:  2013-03-27       Impact factor: 2.415

3.  Radical cascades using enantioenriched 7-azabenzonorbornenes and their applications in synthesis.

Authors:  David M Hodgson; Leonard H Winning
Journal:  Beilstein J Org Chem       Date:  2008-10-24       Impact factor: 2.883

4.  Stereoselective Synthesis of Tropanes via a 6π-Electrocyclic Ring-Opening/ Huisgen [3+2]-Cycloaddition Cascade of Monocyclopropanated Heterocycles.

Authors:  Carina M Sonnleitner; Saerom Park; Robert Eckl; Thomas Ertl; Oliver Reiser
Journal:  Angew Chem Int Ed Engl       Date:  2020-08-18       Impact factor: 15.336

  4 in total

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