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Journal Abstract Search

536 related items for PubMed ID: 23627257

  • 1. An asymmetric Michael addition of α,α-disubstituted aldehydes to maleimides leading to a one-pot enantioselective synthesis of lactones catalyzed by amino acids.
    Kokotos CG.
    Org Lett; 2013 May 17; 15(10):2406-9. PubMed ID: 23627257
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  • 3. One-pot asymmetric synthesis of beta-cyanohydroxymethyl alpha-amino acid derivatives: formation of three contiguous stereogenic centers.
    Watanabe S, Córdova A, Tanaka F, Barbas CF.
    Org Lett; 2002 Dec 12; 4(25):4519-22. PubMed ID: 12465927
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  • 8. Enantioselective organocatalytic one-pot amination/aza-Michael/aldol condensation reaction sequence: synthesis of 3-pyrrolines with a quaternary stereocenter.
    Desmarchelier A, Coeffard V, Moreau X, Greck C.
    Chemistry; 2012 Oct 08; 18(41):13222-5. PubMed ID: 22927036
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  • 11. Diphenylprolinol silyl ether catalyzed asymmetric Michael reaction of nitroalkanes and β,β-disubstituted α,β-unsaturated aldehydes for the construction of all-carbon quaternary stereogenic centers.
    Hayashi Y, Kawamoto Y, Honda M, Okamura D, Umemiya S, Noguchi Y, Mukaiyama T, Sato I.
    Chemistry; 2014 Sep 15; 20(38):12072-82. PubMed ID: 25164711
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  • 16. Catalytic asymmetric synthesis of trans-configured beta-lactones: cooperation of Lewis acid and ion pair catalysis.
    Kull T, Cabrera J, Peters R.
    Chemistry; 2010 Aug 09; 16(30):9132-9. PubMed ID: 20602368
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  • 17. Asymmetric Michael addition of α-substituted isocyanoacetates with maleimides catalyzed by chiral tertiary amine thiourea.
    Bai JF, Wang LL, Peng L, Guo YL, Jia LN, Tian F, He GY, Xu XY, Wang LX.
    J Org Chem; 2012 Mar 16; 77(6):2947-53. PubMed ID: 22369654
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  • 19. Direct synthesis of β-hydroxy-α-amino acids via diastereoselective decarboxylative aldol reaction.
    Singjunla Y, Baudoux J, Rouden J.
    Org Lett; 2013 Nov 15; 15(22):5770-3. PubMed ID: 24188057
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  • 20. Peptide-Catalyzed Stereoselective Conjugate Addition Reaction of Aldehydes to C-Substituted Maleimides.
    Vastakaite G, Grünenfelder CE, Wennemers H.
    Chemistry; 2022 Mar 28; 28(18):e202200215. PubMed ID: 35089626
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