Literature DB >> 31245793

On the Winstein rearrangement: equilibrium and mechanism.

Amy A Ott1, Joseph J Topczewski1.   

Abstract

Allylic azides are underutilized in organic synthesis when compared to other organic azides or other allylic functionality. This is likely because allylic azides rearrange at room temperature, resulting in a potentially complex mixture of azides. This rearrangement has been termed the Winstein rearrangement. Understanding the mechanism and basic principles governing the allylic azide equilibrium may aid in developing applications for these molecules based on either alkene or azide functionalization. Presented herein is a compilation of the key observations regarding the nature of the allylic azide rearrangement. Mechanistic considerations are explicitly addressed with key examples from the literature.

Entities:  

Keywords:  Azides; equilibrium; mechanism; sigmatropic

Year:  2019        PMID: 31245793      PMCID: PMC6594568          DOI: 10.24820/ark.5550190.p010.819

Source DB:  PubMed          Journal:  ARKIVOC            Impact factor:   1.140


  14 in total

1.  Sterically biased 3,3-sigmatropic rearrangement of chiral allylic azides: application to the total syntheses of alkaloids.

Authors:  Sophie Lauzon; François Tremblay; David Gagnon; Cédrickx Godbout; Christine Chabot; Catherine Mercier-Shanks; Stéphane Perreault; Hélène DeSève; Claude Spino
Journal:  J Org Chem       Date:  2008-07-22       Impact factor: 4.354

2.  Sterically biased 3,3-sigmatropic rearrangement of azides: efficient preparation of nonracemic alpha-amino acids and heterocycles.

Authors:  David Gagnon; Sophie Lauzon; Cédrickx Godbout; Claude Spino
Journal:  Org Lett       Date:  2005-10-13       Impact factor: 6.005

3.  The allylic azide rearrangement: achieving selectivity.

Authors:  Alina K Feldman; Benoît Colasson; K Barry Sharpless; Valery V Fokin
Journal:  J Am Chem Soc       Date:  2005-10-05       Impact factor: 15.419

4.  Claisen rearrangements of equilibrating allylic azides.

Authors:  Donald Craig; John W Harvey; Alexander G O'Brien; Andrew J P White
Journal:  Org Biomol Chem       Date:  2011-08-30       Impact factor: 3.876

5.  Stereocontrol in a combined allylic azide rearrangement and intramolecular Schmidt reaction.

Authors:  Ruzhang Liu; Osvaldo Gutierrez; Dean J Tantillo; Jeffrey Aubé
Journal:  J Am Chem Soc       Date:  2012-04-10       Impact factor: 15.419

6.  Dynamic Kinetic Resolution of Allylic Azides via Asymmetric Dihydroxylation.

Authors:  Amy A Ott; Charles S Goshey; Joseph J Topczewski
Journal:  J Am Chem Soc       Date:  2017-06-05       Impact factor: 15.419

7.  Organic azides: an exploding diversity of a unique class of compounds.

Authors:  Stefan Bräse; Carmen Gil; Kerstin Knepper; Viktor Zimmermann
Journal:  Angew Chem Int Ed Engl       Date:  2005-08-19       Impact factor: 15.336

8.  Allylic Azide Rearrangement in Tandem with Huisgen Cycloaddition for Stereoselective Annulation: Synthesis of C-Glycosyl Iminosugars.

Authors:  Lorna Moynihan; Rekha Chadda; Patrick McArdle; Paul V Murphy
Journal:  Org Lett       Date:  2015-12-09       Impact factor: 6.005

9.  Enantioselective, Stereodivergent Hydroazidation and Hydroamination of Allenes Catalyzed by Acyclic Diaminocarbene (ADC) Gold(I) Complexes.

Authors:  Dimitri A Khrakovsky; Chuanzhou Tao; Miles W Johnson; Richard T Thornbury; Sophia L Shevick; F Dean Toste
Journal:  Angew Chem Int Ed Engl       Date:  2016-04-20       Impact factor: 15.336

10.  A concomitant allylic azide rearrangement/intramolecular azide-alkyne cycloaddition sequence.

Authors:  Rakesh H Vekariya; Ruzhang Liu; Jeffrey Aubé
Journal:  Org Lett       Date:  2014-03-17       Impact factor: 6.005

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  5 in total

1.  Divergent Mechanisms of the Banert Cascade with Propargyl Azides.

Authors:  Juliana R Alexander; Mary H Packard; Alanna M Hildebrandt; Amy A Ott; Joseph J Topczewski
Journal:  J Org Chem       Date:  2020-01-24       Impact factor: 4.354

2.  Intercepting the Banert cascade with nucleophilic fluorine: direct access to α-fluorinated NH-1,2,3-triazoles.

Authors:  J R Alexander; P V Kevorkian; J J Topczewski
Journal:  Chem Commun (Camb)       Date:  2021-05-20       Impact factor: 6.222

3.  Enantioselective Nickel-Catalyzed Alkyne-Azide Cycloaddition by Dynamic Kinetic Resolution.

Authors:  En-Chih Liu; Joseph J Topczewski
Journal:  J Am Chem Soc       Date:  2021-04-02       Impact factor: 15.419

4.  A cascade reaction of cinnamyl azides with vinyl sulfones directly generates dihydro-pyrrolo-pyrazole heterocycles.

Authors:  Angela S Carlson; Alexandru M Petre; Joseph J Topczewski
Journal:  Tetrahedron Lett       Date:  2021-02-03       Impact factor: 2.415

5.  Insight into the factors controlling the equilibrium of allylic azides.

Authors:  Margarita M Vallejos; Guillermo R Labadie
Journal:  RSC Adv       Date:  2020-01-27       Impact factor: 4.036

  5 in total

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