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 *

93 related articles for article (PubMed ID: 29334463)

  • 1. Torquoselective Mechanochemical Activation of the Staudinger Reaction To Form β-Lactams.
    Marx D; Menéndez MI
    J Org Chem; 2018 Feb; 83(4):2438-2441. PubMed ID: 29334463
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The mechanism of the ketene-imine (staudinger) reaction in its centennial: still an unsolved problem?
    Cossío FP; Arrieta A; Sierra MA
    Acc Chem Res; 2008 Aug; 41(8):925-36. PubMed ID: 18662024
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New insights into the torquoselectivity of the Staudinger reaction.
    Liang Y; Jiao L; Zhang S; Yu ZX; Xu J
    J Am Chem Soc; 2009 Feb; 131(4):1542-9. PubMed ID: 19132931
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Retro-Staudinger Cycloaddition: Mechanochemical Cycloelimination of a β-Lactam Mechanophore.
    Robb MJ; Moore JS
    J Am Chem Soc; 2015 Sep; 137(34):10946-9. PubMed ID: 26295609
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Electronic origins of the stereochemistry in β-lactam formed through the Staudinger reaction catalyzed by a nucleophile.
    Pahlavan F; Moosavi SS; Zolghadr AR; Iranpoor N
    RSC Adv; 2023 Nov; 13(48):33654-33667. PubMed ID: 38020014
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Origin of the relative stereoselectivity of the beta-lactam formation in the Staudinger reaction.
    Jiao L; Liang Y; Xu J
    J Am Chem Soc; 2006 May; 128(18):6060-9. PubMed ID: 16669675
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Stereoselective control in the Staudinger reactions involving monosubstituted ketenes with electron acceptor substituents: experimental investigation and theoretical rationalization.
    Qi H; Li X; Xu J
    Org Biomol Chem; 2011 Apr; 9(8):2702-14. PubMed ID: 21359284
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Do reaction conditions affect the stereoselectivity in the Staudinger reaction?
    Wang Y; Liang Y; Jiao L; Du DM; Xu J
    J Org Chem; 2006 Sep; 71(18):6983-90. PubMed ID: 16930052
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diastereoselectivity in the Staudinger reaction of pentafluorosulfanylaldimines and ketimines.
    Penger A; von Hahmann CN; Filatov AS; Welch JT
    Beilstein J Org Chem; 2013; 9():2675-80. PubMed ID: 24367432
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stereocontrolled synthesis of anticancer beta-lactams via the Staudinger reaction.
    Banik BK; Banik I; Becker FF
    Bioorg Med Chem; 2005 Jun; 13(11):3611-22. PubMed ID: 15862989
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New insights on the origins of the stereocontrol of the staudinger reaction: [2 + 2] cycloaddition between ketenes and N-silylimines.
    Arrieta A; Cossío FP; Lecea B
    J Org Chem; 2000 Dec; 65(25):8458-64. PubMed ID: 11112564
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mixed carboxylic-sulfonic anhydride in reaction with imines: a straightforward route to water-soluble β-lactams via a Staudinger-type reaction.
    Bakulina O; Dar'in D; Krasavin M
    Org Biomol Chem; 2018 May; 16(21):3989-3998. PubMed ID: 29766192
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Explorations on the total synthesis of the unusual marine alkaloid chartelline A.
    Sun C; Lin X; Weinreb SM
    J Org Chem; 2006 Apr; 71(8):3159-66. PubMed ID: 16599614
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 12- to 22-membered bridged β-lactams as potential penicillin-binding protein inhibitors.
    Sliwa A; Dive G; Marchand-Brynaert J
    Chem Asian J; 2012 Feb; 7(2):425-34. PubMed ID: 22162344
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis of β-lactams by transition metal promoted Staudinger reactions: alternative synthetic approaches from transition metal enhanced organocatalysis to in situ, highly reactive intermediate synthesis and catalytic tandem reactions.
    Tuba R
    Org Biomol Chem; 2013 Sep; 11(36):5976-88. PubMed ID: 23925443
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Staudinger reaction with 2-imino-1,3-thiaselenanes toward the synthesis of C4 spiro-β-lactams.
    Toyoda Y; Ninomiya M; Ebihara M; Koketsu M
    Org Biomol Chem; 2013 Apr; 11(16):2652-9. PubMed ID: 23460025
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diastereoselective synthesis of potent antimalarial cis-β-lactam agents through a [2 + 2] cycloaddition of chiral imines with a chiral ketene.
    Jarrahpour A; Ebrahimi E; Sinou V; Latour C; Brunel JM
    Eur J Med Chem; 2014 Nov; 87():364-71. PubMed ID: 25282260
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Competing thermal electrocyclic ring-closure reactions of (2Z)-hexa-2,4,5-trienals and their Schiff bases. Structural, kinetic, and computational studies.
    Souto JA; Pérez M; Silva López C; Alvarez R; Torrado A; de Lera AR
    J Org Chem; 2010 Jul; 75(13):4453-62. PubMed ID: 20521841
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Synthesis of highly substituted cyclobutane fused-ring systems from N-vinyl beta-lactams through a one-pot domino process.
    Cheung LL; Yudin AK
    Chemistry; 2010 Apr; 16(13):4100-9. PubMed ID: 20186912
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Relative reactivity of three and four membered rings--the absence of charge effect.
    Wolk JL; Sprecher M; Basch H; Hoz S
    Org Biomol Chem; 2004 Apr; 2(7):1065-9. PubMed ID: 15034630
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.