Simon Jones

Summary

Affiliation: University of Sheffield
Country: UK

Publications

  1. ncbi request reprint Highly diastereoselective Diels-Alder cycloadditions of 9R-(1-methoxyethyl)anthracene with p-benzoquinone
    Harry Adams
    Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, UK
    Org Biomol Chem 4:2296-303. 2006
  2. doi request reprint Diastereoselective cycloadditions and transformations of N-alkyl and N-aryl maleimides with chiral 9-anthrylethanol derivatives
    Harry Adams
    Department of Chemistry, Dainton Building, University of Sheffield, Brook Hill, Sheffield S3 7HF, UK
    J Org Chem 75:6252-62. 2010
  3. ncbi request reprint Trichlorosilane mediated asymmetric reductions of the C=N bond
    Simon Jones
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield S3 7HF, UK
    Org Biomol Chem 10:2189-200. 2012
  4. doi request reprint Asymmetric reduction of ketimines with trichlorosilane employing an imidazole derived organocatalyst
    François Moana Gautier
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield, UKS3 7HF
    Org Biomol Chem 7:229-31. 2009
  5. doi request reprint Scope of the organocatalysed asymmetric reductive amination of ketones with trichlorosilane
    François Moana Gautier
    Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, UK S3 7HF
    Org Biomol Chem 9:7860-8. 2011
  6. doi request reprint Asymmetric synthesis of corsifuran A by an enantioselective oxazaborolidine reduction
    Harry Adams
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield S6 1XD, UK
    Org Lett 10:1457-60. 2008
  7. ncbi request reprint N-alkyl oxazolidines as stereocontrol elements in asymmetric Diels-Alder cycloadditions of 9-substituted anthracene derivatives
    Harry Adams
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield, UK
    Org Biomol Chem 4:4206-13. 2006
  8. doi request reprint Hydrogen production from formic acid decomposition at room temperature using a Ag-Pd core-shell nanocatalyst
    Karaked Tedsree
    Wolfson Catalysis Centre, Department of Chemistry, University of Oxford, Oxford, OX1 3QR, UK
    Nat Nanotechnol 6:302-7. 2011
  9. ncbi request reprint Enantioselective preparation of p-chiral phosphine oxides
    Harry Adams
    Department of Chemistry, Dainton Building, University of Sheffield, Brook Hill, Sheffield, S3 7HF, U K
    Org Lett 13:6576-9. 2011
  10. doi request reprint Synthesis of quaternary stereogenic centres via stereoselective intermolecular Friedel-Crafts reactions
    Jennifer C Ball
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield, S3 7HF, UK
    Org Biomol Chem 9:4353-60. 2011

Collaborators

  • Harry Adams
  • François Moana Gautier
  • Nathan J Gilmore
  • Karaked Tedsree
  • Jennifer C Ball
  • Stephen J Martin
  • Isaac Ojea-Jimenez
  • Mark P Muldowney
  • Christopher J A Warner
  • Xianfu Li
  • Paul A J Bagot
  • Emmanuelle A Marquis
  • Rebecca C Collins
  • Robert Gleave
  • Shik Chi Edman Tsang
  • George D W Smith
  • Kai Man Kerry Yu
  • Tong Li
  • Chun Wong Aaron Chan
  • Tareg M Elsunaki
  • Anthony J H M Meijer
  • Ramesh Vemula
  • Stephan H von Reuss
  • Ramadan A Bawa

Detail Information

Publications11

  1. ncbi request reprint Highly diastereoselective Diels-Alder cycloadditions of 9R-(1-methoxyethyl)anthracene with p-benzoquinone
    Harry Adams
    Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, UK
    Org Biomol Chem 4:2296-303. 2006
    ..Mechanistic studies to explore the origins of this selectivity have shown that at lower temperatures the kinetic product predominates, giving a 96:4 ratio of cycloadducts...
  2. doi request reprint Diastereoselective cycloadditions and transformations of N-alkyl and N-aryl maleimides with chiral 9-anthrylethanol derivatives
    Harry Adams
    Department of Chemistry, Dainton Building, University of Sheffield, Brook Hill, Sheffield S3 7HF, UK
    J Org Chem 75:6252-62. 2010
    ..Computational studies supported the proposed hypotheses for the stereoselectivity observed in the transformations described...
  3. ncbi request reprint Trichlorosilane mediated asymmetric reductions of the C=N bond
    Simon Jones
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield S3 7HF, UK
    Org Biomol Chem 10:2189-200. 2012
    ..In this perspective, we wish to highlight the progress made in the past decade in this field and offer a direct quantitative comparison to transition-metal mediated process...
  4. doi request reprint Asymmetric reduction of ketimines with trichlorosilane employing an imidazole derived organocatalyst
    François Moana Gautier
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield, UKS3 7HF
    Org Biomol Chem 7:229-31. 2009
    ....
  5. doi request reprint Scope of the organocatalysed asymmetric reductive amination of ketones with trichlorosilane
    François Moana Gautier
    Department of Chemistry, University of Sheffield, Brook Hill, Sheffield, UK S3 7HF
    Org Biomol Chem 9:7860-8. 2011
    ..The efficient synthesis of the calcimimetic (+)-NPS R-568 (67%, 89% ee) demonstrated the synthetic applicability of this methodology...
  6. doi request reprint Asymmetric synthesis of corsifuran A by an enantioselective oxazaborolidine reduction
    Harry Adams
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield S6 1XD, UK
    Org Lett 10:1457-60. 2008
    ..Corsifuran A has been prepared in an enantiomerically pure form for the first time by an asymmetric reduction procedure, allowing confirmation of the absolute stereochemistry of the natural product as (R)...
  7. ncbi request reprint N-alkyl oxazolidines as stereocontrol elements in asymmetric Diels-Alder cycloadditions of 9-substituted anthracene derivatives
    Harry Adams
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield, UK
    Org Biomol Chem 4:4206-13. 2006
    ..Asymmetric Diels-Alder cycloadditions of these with N-methyl maleimide proceeds in good yield and in good diastereoselectivity, the sense of which may be controlled by judicious choice of the N-alkyl group...
  8. doi request reprint Hydrogen production from formic acid decomposition at room temperature using a Ag-Pd core-shell nanocatalyst
    Karaked Tedsree
    Wolfson Catalysis Centre, Department of Chemistry, University of Oxford, Oxford, OX1 3QR, UK
    Nat Nanotechnol 6:302-7. 2011
    ..Our nanocatalysts could be used in the development of micro polymer electrolyte membrane fuel cells for portable devices and could also be applied in the promotion of other catalytic reactions under mild conditions...
  9. ncbi request reprint Enantioselective preparation of p-chiral phosphine oxides
    Harry Adams
    Department of Chemistry, Dainton Building, University of Sheffield, Brook Hill, Sheffield, S3 7HF, U K
    Org Lett 13:6576-9. 2011
    ..The methodology involves the highly stereoselective formation of P-chiral oxazolidinones that then undergo displacement with a variety of Grignard reagents to prepare the desired phosphine oxides...
  10. doi request reprint Synthesis of quaternary stereogenic centres via stereoselective intermolecular Friedel-Crafts reactions
    Jennifer C Ball
    Department of Chemistry, University of Sheffield, Dainton Building, Brook Hill, Sheffield, S3 7HF, UK
    Org Biomol Chem 9:4353-60. 2011
    ..Retro-Diels-Alder reaction of one of the reaction products led to a precursor that could be used for the construction of pyroglutamic acids bearing quaternary stereogenic centres...
  11. ncbi request reprint Synthetic applicability and in situ recycling of a B-methoxy oxazaborolidine catalyst derived from cis-1-amino-indan-2-ol
    Nathan J Gilmore
    Department of Chemistry, Dainton Building, University of Sheffield, Sheffield, Brook Hill, Sheffield S3 7HF, UK
    Org Lett 6:2805-8. 2004
    ..A method for reducing the effective catalyst loading by "in situ recycling" is also presented. [structure: see text]..