These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 32329616)

  • 1. Deactivation of Secondary Amine Catalysts via Aldol Reaction-Amine Catalysis under Solvent-Free Conditions.
    Schnitzer T; Wennemers H
    J Org Chem; 2020 Jun; 85(12):7633-7640. PubMed ID: 32329616
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Overcoming Deactivation of Amine-Based Catalysts: Access to Fluoroalkylated γ-Nitroaldehydes.
    Schnurr M; Rackl JW; Wennemers H
    J Am Chem Soc; 2023 Oct; 145(42):23275-23280. PubMed ID: 37845230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The diarylprolinol silyl ether system: a general organocatalyst.
    Jensen KL; Dickmeiss G; Jiang H; Albrecht L; Jørgensen KA
    Acc Chem Res; 2012 Feb; 45(2):248-64. PubMed ID: 21848275
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Di(methylimidazole)prolinol silyl ether catalyzed highly Michael addition of aldehydes to nitroolefins in water.
    Wu J; Ni B; Headley AD
    Org Lett; 2009 Aug; 11(15):3354-6. PubMed ID: 19572597
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adapting to substrate challenges: peptides as catalysts for conjugate addition reactions of aldehydes to α,β-disubstituted nitroolefins.
    Duschmalé J; Wennemers H
    Chemistry; 2012 Jan; 18(4):1111-20. PubMed ID: 22189758
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tripeptides of the type H-D-Pro-Pro-Xaa-NH2 as catalysts for asymmetric 1,4-addition reactions: structural requirements for high catalytic efficiency.
    Wiesner M; Neuburger M; Wennemers H
    Chemistry; 2009 Oct; 15(39):10103-9. PubMed ID: 19697376
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Enamine catalysis with low catalyst loadings--high efficiency via kinetic studies.
    Wiesner M; Upert G; Angelici G; Wennemers H
    J Am Chem Soc; 2010 Jan; 132(1):6-7. PubMed ID: 19791790
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Primary amine-metal Lewis acid bifunctional catalysts based on a simple bidentate ligand: direct asymmetric aldol reaction.
    Daka P; Xu Z; Alexa A; Wang H
    Chem Commun (Camb); 2011 Jan; 47(1):224-6. PubMed ID: 20563349
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Amine-catalyzed enantioselective 1,3-dipolar cycloadditions of aldehydes to C,N-cyclic azomethine imines.
    Li W; Jia Q; Du Z; Zhang K; Wang J
    Chemistry; 2014 Apr; 20(16):4559-62. PubMed ID: 24644273
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Peptide-Catalyzed Stereoselective Conjugate Addition Reaction of Aldehydes to C-Substituted Maleimides.
    Vastakaite G; Grünenfelder CE; Wennemers H
    Chemistry; 2022 Mar; 28(18):e202200215. PubMed ID: 35089626
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Catalyst Control over Twofold and Higher-Order Stereogenicity by Atroposelective Arene Formation.
    Schmidt TA; Sparr C
    Acc Chem Res; 2021 Jun; 54(12):2764-2774. PubMed ID: 34056908
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Heterogeneous dehydrocoupling of amine-borane adducts by skeletal nickel catalysts.
    Robertson AP; Suter R; Chabanne L; Whittell GR; Manners I
    Inorg Chem; 2011 Dec; 50(24):12680-91. PubMed ID: 22103654
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transition states of amine-catalyzed aldol reactions involving enamine intermediates: theoretical studies of mechanism, reactivity, and stereoselectivity.
    Bahmanyar S; Houk KN
    J Am Chem Soc; 2001 Nov; 123(45):11273-83. PubMed ID: 11697970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Peptide-Catalyzed Stereoselective Conjugate Addition Reactions of Aldehydes to Maleimide.
    Grünenfelder CE; Kisunzu JK; Wennemers H
    Angew Chem Int Ed Engl; 2016 Jul; 55(30):8571-4. PubMed ID: 27254460
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amine Catalysis with Substrates Bearing N-Heterocyclic Moieties Enabled by Control over the Enamine Pyramidalization Direction.
    Möhler JS; Schnitzer T; Wennemers H
    Chemistry; 2020 Dec; 26(67):15623-15628. PubMed ID: 32573875
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Triflimide: An Overlooked High-Performance Catalyst of the Mukaiyama Aldol Reaction of Silyl Ketene Acetals with Ketones.
    Bae HY; List B
    Chemistry; 2018 Sep; 24(52):13767-13772. PubMed ID: 29943495
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Peptide and Enzyme Catalysts Work in Concert in Stereoselective Cascade Reactions-Oxidation followed by Conjugate Addition.
    Möhler JS; Pickl M; Reiter T; Simić S; Rackl JW; Kroutil W; Wennemers H
    Angew Chem Int Ed Engl; 2024 Mar; 63(12):e202319457. PubMed ID: 38235524
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Increased structural complexity leads to higher activity: peptides as efficient and versatile catalysts for asymmetric aldol reactions.
    Krattiger P; Kovasy R; Revell JD; Ivan S; Wennemers H
    Org Lett; 2005 Mar; 7(6):1101-3. PubMed ID: 15760149
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Density functional study of organocatalytic cross-aldol reactions between two aliphatic aldehydes: insight into their functional differentiation and origins of chemo- and stereoselectivities.
    Fu A; Zhao C; Li H; Tian F; Yuan S; Duan Y; Wang Z
    J Phys Chem A; 2013 Apr; 117(13):2862-72. PubMed ID: 23442005
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bifunctional Iminophosphorane Superbase Catalysis: Applications in Organic Synthesis.
    Formica M; Rozsar D; Su G; Farley AJM; Dixon DJ
    Acc Chem Res; 2020 Oct; 53(10):2235-2247. PubMed ID: 32886474
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.