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 *

107 related articles for article (PubMed ID: 37392432)

  • 1. Sulfamidate-Based Stereoselective Total Synthesis of (+)-Preussin Using Gold(I)-Catalyzed Intramolecular Dehydrative Amination: Dead End and Detour.
    Park Y; Ryu JS
    J Org Chem; 2023 Jul; 88(14):9902-9909. PubMed ID: 37392432
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stereoselective Synthesis of Functionalized 1,3-Disubstituted Isoindolines via Rh(III)-Catalyzed Tandem Oxidative Olefination-Cyclization of 4-Aryl-cyclic Sulfamidate-5-Carboxylates.
    Achary R; Jung IA; Son SM; Lee HK
    J Org Chem; 2017 Jul; 82(14):7223-7233. PubMed ID: 28670904
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Stereoselective synthesis of 1,3-disubstituted isoindolines via Rh(III)-catalyzed tandem oxidative olefination-cyclization of 4-aryl cyclic sulfamidates.
    Son SM; Seo YJ; Lee HK
    Chem Commun (Camb); 2016 Mar; 52(23):4286-9. PubMed ID: 26841961
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Formal Synthesis of (+)-Laurencin by Gold(I)-Catalyzed Intramolecular Dehydrative Alkoxylation.
    Lanier ML; Park H; Mukherjee P; Timmerman JC; Ribeiro AA; Widenhoefer RA; Hong J
    Chemistry; 2017 May; 23(30):7180-7184. PubMed ID: 28393406
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DBU-Promoted Dynamic Kinetic Resolution in Rh-Catalyzed Asymmetric Transfer Hydrogenation of 5-Alkyl Cyclic Sulfamidate Imines: Stereoselective Synthesis of Functionalized 1,2-Amino Alcohols.
    Kim HR; Achary R; Lee HK
    J Org Chem; 2018 Oct; 83(19):11987-11999. PubMed ID: 30199258
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Five-membered cyclic sulfamidate imines: versatile scaffolds for organic synthesis.
    Pham QH; Hyland CJT; Pyne SG
    Org Biomol Chem; 2020 Oct; 18(38):7467-7484. PubMed ID: 32930695
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis of Fluorescent Lanthipeptide Cytolysin S Analogues by Late-Stage Sulfamidate Ring Opening.
    Mazo N; Rahman IR; Navo CD; Peregrina JM; Busto JH; van der Donk WA; Jiménez-Osés G
    Org Lett; 2023 Mar; 25(9):1431-1435. PubMed ID: 36849130
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A concise stereoselective synthesis of Preussin, 3-epi-Preussin, and analogues.
    Bertrand MB; Wolfe JP
    Org Lett; 2006 May; 8(11):2353-6. PubMed ID: 16706524
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel multistep mechanism for the stereocontrolled ring opening of hindered sulfamidates: mild, green, and efficient reactivity with alcohols.
    Jiménez-Osés G; Avenoza A; Busto JH; Rodríguez F; Peregrina JM
    Chemistry; 2009 Sep; 15(38):9810-23. PubMed ID: 19681068
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rhodium(II)-catalyzed alkyne amination of homopropargylic sulfamate esters: stereoselective synthesis of functionalized norcaradienes by arene cyclopropanation.
    Brawn RA; Zhu K; Panek JS
    Org Lett; 2014 Jan; 16(1):74-7. PubMed ID: 24328560
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Silver- and gold-catalyzed intramolecular rearrangement of propargylic alcohols tethered with methylenecyclopropanes: stereoselective synthesis of allenylcyclobutanols and 1-vinyl-3-oxabicyclo[3.2.1]octan-8-one derivatives.
    Yao LF; Wei Y; Shi M
    J Org Chem; 2009 Dec; 74(24):9466-9. PubMed ID: 19916486
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis of β
    Tovillas P; Navo CD; Oroz P; Avenoza A; Corzana F; Zurbano MM; Jiménez-Osés G; Busto JH; Peregrina JM
    J Org Chem; 2022 Jul; 87(13):8730-8743. PubMed ID: 35732024
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis of l-[4-
    Xu Y; Cankaya AS; Hoque R; Lee SJ; Shea C; Kersting L; Schueller M; Fowler JS; Szalda D; Alexoff D; Riehl B; Gleede T; Ferrieri RA; Qu W
    Chemistry; 2018 May; 24(26):6848-6853. PubMed ID: 29504637
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gold(I)-catalyzed enantioselective intramolecular dehydrative amination of allylic alcohols with carbamates.
    Mukherjee P; Widenhoefer RA
    Angew Chem Int Ed Engl; 2012 Feb; 51(6):1405-7. PubMed ID: 22294357
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stereoselective Synthesis of 3,3-Disubstituted Oxindoles and Spirooxindoles via Allylic Alkylation of Morita-Baylis-Hillman Carbonates of Isatins with Cyclic Sulfamidate Imines Catalyzed by DABCO.
    Arupula SK; Guin S; Yadav A; Mobin SM; Samanta S
    J Org Chem; 2018 Mar; 83(5):2660-2675. PubMed ID: 29412661
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Iridium-catalyzed allylic vinylation and asymmetric allylic amination reactions with o-aminostyrenes.
    Ye KY; He H; Liu WB; Dai LX; Helmchen G; You SL
    J Am Chem Soc; 2011 Nov; 133(46):19006-14. PubMed ID: 21995503
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gold-catalyzed intramolecular allylic amination of 2-tosylaminophenylprop-1-en-3-ols. A concise synthesis of (+/-)-angustureine.
    Kothandaraman P; Foo SJ; Chan PW
    J Org Chem; 2009 Aug; 74(16):5947-52. PubMed ID: 19603765
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Three-step synthesis of (±)-preussin from decanal.
    Rosset IG; Dias RM; Pinho VD; Burtoloso AC
    J Org Chem; 2014 Jul; 79(14):6748-53. PubMed ID: 24979222
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Applications of Iridium-Catalyzed Asymmetric Allylic Substitution Reactions in Target-Oriented Synthesis.
    Qu J; Helmchen G
    Acc Chem Res; 2017 Oct; 50(10):2539-2555. PubMed ID: 28937739
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis of Mixed α/β2,2-Peptides by Site-Selective Ring-Opening of Cyclic Quaternary Sulfamidates.
    Mazo N; García-González I; Navo CD; Corzana F; Jiménez-Osés G; Avenoza A; Busto JH; Peregrina JM
    Org Lett; 2015 Dec; 17(23):5804-7. PubMed ID: 26569645
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.