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Journal Abstract Search

181 related items for PubMed ID: 27933807

  • 1. Asymmetric Synthesis of γ-Lactones through Koga Amine-Controlled Addition of Enediolates to α,β-Unsaturated Sulfoxonium Salts.
    Peraino NJ, Kaster SH, Wheeler KA, Kerrigan NJ.
    J Org Chem; 2017 Jan 06; 82(1):606-615. PubMed ID: 27933807
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  • 3. Diastereoselective reaction of sulfoxonium ylides, aldehydes and ketenes: an approach to trans-γ-lactones.
    Mondal M, Ho HJ, Peraino NJ, Gary MA, Wheeler KA, Kerrigan NJ.
    J Org Chem; 2013 May 03; 78(9):4587-93. PubMed ID: 23548074
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  • 4. Catalytic Asymmetric Synthesis of Ketene Heterodimer β-Lactones: Scope and Limitations.
    Chen S, Ibrahim AA, Peraino NJ, Nalla D, Mondal M, Van Raaphorst M, Kerrigan NJ.
    J Org Chem; 2016 Sep 02; 81(17):7824-37. PubMed ID: 27490092
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  • 5. Asymmetric α,γ-Regioselective [3 + 3] Formal Cycloadditions of α,β-Unsaturated Aldehydes via Cascade Dienamine-Dienamine Catalysis.
    Xiao W, Yin X, Zhou Z, Du W, Chen YC.
    Org Lett; 2016 Jan 04; 18(1):116-9. PubMed ID: 26653774
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  • 6. An organocatalytic Michael-cyclization cascade of 4-oxa-α,β-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral γ-lactols and trisubstituted γ-lactones.
    Lin JB, Xu SM, Xie JK, Li HY, Xu PF.
    Chem Commun (Camb); 2015 Feb 28; 51(17):3596-9. PubMed ID: 25633800
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  • 7. Phosphine-catalyzed asymmetric synthesis of beta-lactones from arylketoketenes and aromatic aldehydes.
    Mondal M, Ibrahim AA, Wheeler KA, Kerrigan NJ.
    Org Lett; 2010 Apr 16; 12(8):1664-7. PubMed ID: 20337432
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  • 10. Scope and mechanism of tandem aza-Michael reaction/enantioselective protonation using a Pd-μ-hydroxo complex under mild conditions buffered with amine salts.
    Hamashima Y, Suzuki S, Tamura T, Somei H, Sodeoka M.
    Chem Asian J; 2011 Feb 01; 6(2):658-68. PubMed ID: 21254440
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  • 12. A novel chiral sulfonium yilde: highly enantioselective synthesis of vinylcyclopropanes.
    Ye S, Huang ZZ, Xia CA, Tang Y, Dai LX.
    J Am Chem Soc; 2002 Mar 20; 124(11):2432-3. PubMed ID: 11890780
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