A practical and efficient method for the synthesis of .beta.-lactones

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This article has been cited by 17 ACS Journal articles (5 most recent appear below).

• 

  Aryl(trimethylsilyl)selenides as Reagents for the Synthesis of Mono- and Diselenoesters

  Deeb Taher and John F. Corrigan
  Organometallics2011 30 (21), 5943-5952

  • Aryl(trimethylsilyl)selenides as Reagents for the Synthesis of Mono- and Diselenoesters

    Deeb Taher and John F. Corrigan
    Organometallics2011 30 (21), 5943-5952

    Silylated organoselenium reagents react under mild conditions with acid chlorides to provide a high yield route to aromatic selenoesters. The synthesis, structures, and spectroscopic properties of the selenoesters C6H5SeC(O)R (R = CH2CH3, 1; p-CH3C6H4, 2; ...

    Abstract | Full Text HTML | Hi-Res PDF | PDF w/ Links
• 

  NHC-Catalyzed/Titanium(IV)−Mediated Highly Diastereo- and Enantioselective Dimerization of Enals

  Daniel T. Cohen, Benoit Cardinal-David, John M. Roberts, Amy A. Sarjeant, and Karl A. Scheidt
  Organic Letters2011 13 (5), 1068-1071

  • NHC-Catalyzed/Titanium(IV)−Mediated Highly Diastereo- and Enantioselective Dimerization of Enals

    Daniel T. Cohen, Benoit Cardinal-David, John M. Roberts, Amy A. Sarjeant, and Karl A. Scheidt
    Organic Letters2011 13 (5), 1068-1071

    An NHC-catalyzed, diastereo- and enantioselective dimerization of enals has been developed. The use of Ti(Oi-Pr)4 is a key element for the reactivity and selectivity of this process. The cyclopentenes are obtained with high levels of diastereo- and ...

    Abstract | Full Text HTML | Hi-Res PDF | PDF w/ Links
• 

  Catalytic Enantioselective Total Syntheses of Bakkenolides I, J, and S: Application of a Carbene-Catalyzed Desymmetrization

  Eric M. Phillips, John M. Roberts and Karl A. Scheidt
  Organic Letters2010 12 (12), 2830-2833

  • Catalytic Enantioselective Total Syntheses of Bakkenolides I, J, and S: Application of a Carbene-Catalyzed Desymmetrization

    Eric M. Phillips, John M. Roberts and Karl A. Scheidt
    Organic Letters2010 12 (12), 2830-2833

    A general strategy for the catalytic asymmetric syntheses of the bakkenolides is reported. The key bond-forming step involves an N-heterocyclic carbene catalyzed desymmetrization of a 1,3-diketone to form three new bonds in one step with excellent ...

    Abstract | Full Text HTML | Hi-Res PDF | PDF w/ Links
• 

  Aldol-type Reactions of Unmasked Iodoacetic Acid with Carbonyl Compounds Promoted by Samarium Diiodide:  Efficient Synthesis of Carboxylic 3-Hydroxyacids and Their Derivatives

  José M. Concellón and Carmen Concellón
  The Journal of Organic Chemistry2006 71 (12), 4428-4432

  • Aldol-type Reactions of Unmasked Iodoacetic Acid with Carbonyl Compounds Promoted by Samarium Diiodide:  Efficient Synthesis of Carboxylic 3-Hydroxyacids and Their Derivatives

    José M. Concellón and Carmen Concellón
    The Journal of Organic Chemistry2006 71 (12), 4428-4432

    An easy, direct, general, and efficient samarium diiodide-mediated preparation of 3-hydroxyacids 1 in high yield by reaction of different aldehydes or ketones with commercially available iodoacetic acid is described. The application of different ...

    Abstract | Full Text HTML | Hi-Res PDF | PDF w/ Links
• 

  Anionic Inverse Electron-Demand 1,3-Dipolar Cycloaddition of Nitrones with Ynolates. Facile Stereoselective Synthesis of 5-Isoxazolidinones Leading to β-Amino Acids

  Mitsuru Shindo, Kotaro Itoh, Chinatsu Tsuchiya, and Kozo Shishido
  Organic Letters2002 4 (18), 3119-3121

  • Anionic Inverse Electron-Demand 1,3-Dipolar Cycloaddition of Nitrones with Ynolates. Facile Stereoselective Synthesis of 5-Isoxazolidinones Leading to β-Amino Acids

    Mitsuru Shindo, Kotaro Itoh, Chinatsu Tsuchiya, and Kozo Shishido
    Organic Letters2002 4 (18), 3119-3121

    The inverse electron-demand 1,3-dipolar cycloaddition of nitrones with ynolates, followed by quenching with t-BuOH, produced substituted 5-isoxazolidinones with good trans-selectivity. These products were easily converted into β-amino acids.

    Abstract | Full Text HTML | Hi-Res PDF | PDF w/ Links

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