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 *

169 related articles for article (PubMed ID: 37059692)

  • 21. Visible-Light-Induced 1,3-Aminopyridylation of [1.1.1]Propellane with N-Aminopyridinium Salts.
    Shin S; Lee S; Choi W; Kim N; Hong S
    Angew Chem Int Ed Engl; 2021 Mar; 60(14):7873-7879. PubMed ID: 33403785
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Photocatalytic Three-Component Synthesis of 3-Heteroarylbicyclo[1.1.1]pentane-1-acetates.
    Xu W; Zheng Z; Bao G; Wang Y; Gao Y; Zhu H; Xu G; Zhu Y; Yu C; Jiang X
    Org Lett; 2023 Jun; 25(22):4050-4055. PubMed ID: 37235701
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Synthesis of Bicyclo[1.1.1]pentane (BCP)-Based Straight-Shaped Diphosphine Ligands.
    Takano H; Katsuyama H; Hayashi H; Harukawa M; Tsurui M; Shoji S; Hasegawa Y; Maeda S; Mita T
    Angew Chem Int Ed Engl; 2023 Jun; 62(23):e202303435. PubMed ID: 36961369
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sodium Bicyclo[1.1.1]pentanesulfinate: A Bench-Stable Precursor for Bicyclo[1.1.1]pentylsulfones and Bicyclo- [1.1.1]pentanesulfonamides.
    Bär RM; Gross PJ; Nieger M; Bräse S
    Chemistry; 2020 Apr; 26(19):4242-4245. PubMed ID: 31922305
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Iridium-Catalyzed Enantioselective Synthesis of α-Chiral Bicyclo[1.1.1]pentanes by 1,3-Difunctionalization of [1.1.1]Propellane.
    Yu S; Jing C; Noble A; Aggarwal VK
    Org Lett; 2020 Jul; 22(14):5650-5655. PubMed ID: 32638587
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A continuous flow synthesis of [1.1.1]propellane and bicyclo[1.1.1]pentane derivatives.
    Donnelly K; Baumann M
    Chem Commun (Camb); 2021 Mar; 57(23):2871-2874. PubMed ID: 33616143
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Direct catalytic asymmetric synthesis of α-chiral bicyclo[1.1.1]pentanes.
    Wong MLJ; Sterling AJ; Mousseau JJ; Duarte F; Anderson EA
    Nat Commun; 2021 Mar; 12(1):1644. PubMed ID: 33712595
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Rationalizing the diverse reactivity of [1.1.1]propellane through σ-π-delocalization.
    Sterling AJ; Dürr AB; Smith RC; Anderson EA; Duarte F
    Chem Sci; 2020 Apr; 11(19):4895-4903. PubMed ID: 34122945
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Metal-Free Photoredox Four-Component Strategy to 1,3-Functionalized BCP Derivatives.
    Srinivasu V; Das D; Chandu P; Ghosh KG; Sureshkumar D
    Org Lett; 2023 Jul; 25(28):5308-5313. PubMed ID: 37417829
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Synthesis of BCP Benzylamines From 2-Azaallyl Anions and [1.1.1]Propellane.
    Shelp RA; Walsh PJ
    Angew Chem Int Ed Engl; 2018 Nov; 57(48):15857-15861. PubMed ID: 30291667
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exploiting the sp
    Dong W; Yen-Pon E; Li L; Bhattacharjee A; Jolit A; Molander GA
    Nat Chem; 2022 Sep; 14(9):1068-1077. PubMed ID: 35864151
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Photoinduced C(sp3)-H Bicyclopentylation Enabled by an Electron Donor-Acceptor Complex-Mediated Chemoselective Three-Component Radical Relay.
    Dang X; Li Z; Shang J; Zhang C; Wang C; Xu Z
    Angew Chem Int Ed Engl; 2024 Apr; ():e202400494. PubMed ID: 38598042
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Heavy Tetrel Clusters Based on the Bicyclobutane Framework: Bicyclo[1.1.0]butanes, [1.1.1]Propellanes, and Tricyclo[2.1.0.0
    Ya Lee V; Gapurenko OA
    Chem Asian J; 2024 Jan; 19(1):e202300903. PubMed ID: 38015001
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Synthesis of α-Quaternary Bicyclo[1.1.1]pentanes through Synergistic Organophotoredox and Hydrogen Atom Transfer Catalysis.
    Nugent J; Sterling AJ; Frank N; Mousseau JJ; Anderson EA
    Org Lett; 2021 Nov; 23(21):8628-8633. PubMed ID: 34699248
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Organometallic Bridge Diversification of Bicyclo[1.1.1]pentanes.
    Anderson JM; Poole DL; Cook GC; Murphy JA; Measom ND
    Chemistry; 2024 Feb; 30(12):e202304070. PubMed ID: 38117748
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Synthesis and Biological Evaluation of Bicyclo[1.1.1]pentane-Containing Aromatic Lipoxin A
    Owen B; de Gaetano M; Gaffney A; Godson C; Guiry PJ
    Org Lett; 2022 Aug; 24(32):6049-6053. PubMed ID: 35938947
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Aminoalkylation of [1.1.1]Propellane Enables Direct Access to High-Value 3-Alkylbicyclo[1.1.1]pentan-1-amines.
    Hughes JME; Scarlata DA; Chen AC; Burch JD; Gleason JL
    Org Lett; 2019 Sep; 21(17):6800-6804. PubMed ID: 31407916
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Silaboration of [1.1.1]Propellane: A Storable Feedstock for Bicyclo[1.1.1]pentane Derivatives.
    Kondo M; Kanazawa J; Ichikawa T; Shimokawa T; Nagashima Y; Miyamoto K; Uchiyama M
    Angew Chem Int Ed Engl; 2020 Jan; 59(5):1970-1974. PubMed ID: 31603274
    [TBL] [Abstract][Full Text] [Related]  

  • 39. α-Amino bicycloalkylation through organophotoredox catalysis.
    Nugent J; López-Francés A; Sterling AJ; Tay MY; Frank N; Mousseau JJ; Duarte F; Anderson EA
    Chem Sci; 2024 Jul; 15(28):10918-10925. PubMed ID: 39027309
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Large-Scale Synthesis and Modifications of Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid (BCP).
    Ripenko V; Vysochyn D; Klymov I; Zhersh S; Mykhailiuk PK
    J Org Chem; 2021 Oct; 86(20):14061-14068. PubMed ID: 34166594
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.