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 *

138 related articles for article (PubMed ID: 30471673)

  • 1. Homologation of Ugi and Passerini reactions using ynamides.
    Huang B; Cui S
    Drug Discov Today Technol; 2018 Nov; 29():43-49. PubMed ID: 30471673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Keto-Enol Tautomerism in Passerini and Ugi Adducts.
    Pertejo P; Sancho-Medina A; Hermosilla T; González-Saiz B; Gómez-Ayuso J; Quesada R; Moreno D; Carreira-Barral I; García-Valverde M
    Molecules; 2021 Feb; 26(4):. PubMed ID: 33572398
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Single Reactant Replacement Approach of Passerini Reaction: One-Pot Synthesis of β-Acyloxyamides and Phthalides.
    Shen Y; Huang B; Zeng L; Cui S
    Org Lett; 2017 Sep; 19(17):4616-4619. PubMed ID: 28812900
    [TBL] [Abstract][Full Text] [Related]  

  • 4. One-Carbon Homologation of Primary Alcohols to Carboxylic Acids, Esters, and Amides via Mitsunobu Reactions with MAC Reagents.
    Kagawa N; Nibbs AE; Rawal VH
    Org Lett; 2016 May; 18(10):2363-6. PubMed ID: 27135854
    [TBL] [Abstract][Full Text] [Related]  

  • 5. One-Pot Multicomponent Synthesis of β-Amino Amides.
    Huang B; Zeng L; Shen Y; Cui S
    Angew Chem Int Ed Engl; 2017 Apr; 56(16):4565-4568. PubMed ID: 28328156
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Smiles rearrangements in Ugi- and Passerini-type couplings: new multicomponent access to O- and N-arylamides.
    Kaïm LE; Gizolme M; Grimaud L; Oble J
    J Org Chem; 2007 May; 72(11):4169-80. PubMed ID: 17455980
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chiral β
    Zarezin DP; Shmatova OI; Nenajdenko VG
    Org Biomol Chem; 2018 Aug; 16(33):5987-5998. PubMed ID: 30083689
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Borylated reagents for multicomponent reactions.
    Tan J; Yudin AK
    Drug Discov Today Technol; 2018 Nov; 29():51-60. PubMed ID: 30471674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An access to a library of novel triterpene derivatives with a promising pharmacological potential by Ugi and Passerini multicomponent reactions.
    Wiemann J; Heller L; Csuk R
    Eur J Med Chem; 2018 Apr; 150():176-194. PubMed ID: 29529499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New synthetic technology for efficient construction of alpha-hydroxy-beta-amino amides via the Passerini reaction.
    Semple JE; Owens TD; Nguyen K; Levy OE
    Org Lett; 2000 Sep; 2(18):2769-72. PubMed ID: 10964361
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ugi-Smiles couplings: new entries to N-aryl carboxamide derivatives.
    El Kaïm L; Grimaud L
    Mol Divers; 2010 Nov; 14(4):855-67. PubMed ID: 19582586
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Investigation of the Passerini and Ugi reactions in β-lactam aldehydes. Synthetic applications.
    Alcaide B; Almendros P; Aragoncillo C; Callejo R; Ruiz MP; Torres MR
    Org Biomol Chem; 2015 Feb; 13(5):1387-94. PubMed ID: 25460201
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Multicomponent reactions in fungicide research: the discovery of mandipropamid.
    Lamberth C; Jeanguenat A; Cederbaum F; De Mesmaeker A; Zeller M; Kempf HJ; Zeun R
    Bioorg Med Chem; 2008 Feb; 16(3):1531-45. PubMed ID: 17962029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Modular enantioselective access to β-amino amides by Brønsted acid-catalysed multicomponent reactions.
    Wei J; Zhang J; Cheng JK; Xiang SH; Tan B
    Nat Chem; 2023 May; 15(5):647-657. PubMed ID: 37055574
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unconventional Passerini Reaction toward α-Aminoxy-amides.
    Chandgude AL; Dömling A
    Org Lett; 2016 Dec; 18(24):6396-6399. PubMed ID: 27978705
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dual gold catalysis: a novel synthesis of bicyclic and tricyclic pyrroles from N-propargyl ynamides.
    Tokimizu Y; Wieteck M; Rudolph M; Oishi S; Fujii N; Hashmi AS; Ohno H
    Org Lett; 2015 Feb; 17(3):604-7. PubMed ID: 25611870
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Highly regio- and stereoselective trans-iodofluorination of ynamides enabling the synthesis of (E)-α-fluoro-β-iodoenamides.
    Xi Y; Zhu G; Tang L; Ma S; Zhang D; Zhang R; He G; Zhu H
    Org Biomol Chem; 2017 Aug; 15(34):7218-7226. PubMed ID: 28816329
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis, structure, and biological applications of α-fluorinated β-amino acids and derivatives.
    March TL; Johnston MR; Duggan PJ; Gardiner J
    Chem Biodivers; 2012 Nov; 9(11):2410-41. PubMed ID: 23161626
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cleavable β-Cyanoethyl Isocyanide in the Ugi Tetrazole Reaction.
    Kroon E; Kurpiewska K; Kalinowska-Tłuścik J; Dömling A
    Org Lett; 2016 Oct; 18(19):4762-4765. PubMed ID: 27610711
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isocyanide Multicomponent Reactions on Solid Phase: State of the Art and Future Application.
    Cankařová N; Krchňák V
    Int J Mol Sci; 2020 Dec; 21(23):. PubMed ID: 33271974
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.