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 *

115 related articles for article (PubMed ID: 29791161)

  • 1. A Tetrazine-Labile Vinyl Ether Benzyloxycarbonyl Protecting Group (VeZ): An Orthogonal Tool for Solid-Phase Peptide Chemistry.
    Staderini M; Gambardella A; Lilienkampf A; Bradley M
    Org Lett; 2018 Jun; 20(11):3170-3173. PubMed ID: 29791161
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Solid-phase synthesis of asymmetrically branched sequence-defined poly/oligo(amidoamines).
    Wojcik F; Mosca S; Hartmann L
    J Org Chem; 2012 May; 77(9):4226-34. PubMed ID: 22486248
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Coordination-Assisted Bioorthogonal Chemistry: Orthogonal Tetrazine Ligation with Vinylboronic Acid and a Strained Alkene.
    Eising S; Xin BT; Kleinpenning F; Heming JJA; Florea BI; Overkleeft HS; Bonger KM
    Chembiochem; 2018 Aug; 19(15):1648-1652. PubMed ID: 29806887
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inverse electron demand Diels-Alder (IEDDA) reactions in peptide chemistry.
    Pagel M
    J Pept Sci; 2019 Jan; 25(1):e3141. PubMed ID: 30585397
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Efficient labelling of enzymatically synthesized vinyl-modified DNA by an inverse-electron-demand Diels-Alder reaction.
    Busskamp H; Batroff E; Niederwieser A; Abdel-Rahman OS; Winter RF; Wittmann V; Marx A
    Chem Commun (Camb); 2014 Sep; 50(74):10827-9. PubMed ID: 25089682
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New t-butyl based aspartate protecting groups preventing aspartimide formation in Fmoc SPPS.
    Behrendt R; Huber S; Martí R; White P
    J Pept Sci; 2015 Aug; 21(8):680-7. PubMed ID: 26077723
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Building Blocks for the Construction of Bioorthogonally Reactive Peptides via Solid-Phase Peptide Synthesis.
    Zeglis BM; Emmetiere F; Pillarsetty N; Weissleder R; Lewis JS; Reiner T
    ChemistryOpen; 2014 Apr; 3(2):48-53. PubMed ID: 24808990
    [TBL] [Abstract][Full Text] [Related]  

  • 8. On-resin Diels-Alder reaction with inverse electron demand: an efficient ligation method for complex peptides with a varying spacer to optimize cell adhesion.
    Pagel M; Meier R; Braun K; Wiessler M; Beck-Sickinger AG
    Org Biomol Chem; 2016 Jun; 14(21):4809-16. PubMed ID: 27117044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pegylated peptides. II. Solid-phase synthesis of amino-, carboxy- and side-chain pegylated peptides.
    Lu YA; Felix AM
    Int J Pept Protein Res; 1994 Feb; 43(2):127-38. PubMed ID: 8200730
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microwave-assisted cleavage of Alloc and Allyl Ester protecting groups in solid phase peptide synthesis.
    Wilson KR; Sedberry S; Pescatore R; Vinton D; Love B; Ballard S; Wham BC; Hutchison SK; Williamson EJ
    J Pept Sci; 2016 Oct; 22(10):622-627. PubMed ID: 27501347
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Handles for Fmoc solid-phase synthesis of protected peptides.
    Góngora-Benítez M; Tulla-Puche J; Albericio F
    ACS Comb Sci; 2013 May; 15(5):217-28. PubMed ID: 23573835
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis of 'head-to-tail' cyclized peptides on solid support using a chelating amide as new orthogonal protecting group.
    Lay M; Bannwarth W
    J Pept Sci; 2015 Jun; 21(6):461-6. PubMed ID: 25754861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tetrahydropyranyl, a nonaromatic acid-labile Cys protecting group for Fmoc peptide chemistry.
    Ramos-Tomillero I; Rodríguez H; Albericio F
    Org Lett; 2015 Apr; 17(7):1680-3. PubMed ID: 25764355
    [TBL] [Abstract][Full Text] [Related]  

  • 14. New TFA-free cleavage and final deprotection in fmoc solid-phase peptide synthesis: dilute HCl in fluoro alcohol.
    Palladino P; Stetsenko DA
    Org Lett; 2012 Dec; 14(24):6346-9. PubMed ID: 23210918
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fmoc-Sec(Xan)-OH: synthesis and utility of Fmoc selenocysteine SPPS derivatives with acid-labile sidechain protection.
    Flemer S
    J Pept Sci; 2015 Jan; 21(1):53-9. PubMed ID: 25504629
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tetrazine cyclized peptides for one-bead-one-compound library: Synthesis and sequencing.
    Das S; Nag A
    Methods Enzymol; 2024; 698():141-167. PubMed ID: 38886030
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two novel 1,2,4,5-tetrazines that participate in inverse electron demand Diels-Alder reactions with an unexpected regioselectivity.
    Hamasaki A; Ducray R; Boger DL
    J Org Chem; 2006 Jan; 71(1):185-93. PubMed ID: 16388634
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Development of orthogonally protected hypusine for solid-phase peptide synthesis.
    Song A; Tom J; Yu Z; Pham V; Tan D; Zhang D; Fang G; Yu T; Deshayes K
    J Org Chem; 2015 Apr; 80(7):3677-81. PubMed ID: 25769022
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chiral tertiary amine thiourea-catalyzed asymmetric inverse-electron-demand Diels-Alder reaction of chromone heterodienes using 3-vinylindoles as dienophiles.
    Mao Z; Lin A; Shi Y; Mao H; Li W; Cheng Y; Zhu C
    J Org Chem; 2013 Oct; 78(20):10233-9. PubMed ID: 24007305
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis and inverse electron demand Diels-Alder reactions of 3,6-bis(3,4-dimethoxybenzoyl)-1,2,4,5-tetrazine.
    Soenen DR; Zimpleman JM; Boger DL
    J Org Chem; 2003 May; 68(9):3593-8. PubMed ID: 12713365
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.