BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 35726789)

  • 1. The ultimate Lewis acid catalyst: using tris(pentafluorophenyl) borane to create bespoke siloxane architectures.
    Gao H; Battley A; Leitao EM
    Chem Commun (Camb); 2022 Jul; 58(54):7451-7465. PubMed ID: 35726789
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tris(pentafluorophenyl)borane-catalyzed Hydride Transfer Reactions in Polysiloxane Chemistry-Piers-Rubinsztajn Reaction and Related Processes.
    Rubinsztajn S; Chojnowski J; Mizerska U
    Molecules; 2023 Aug; 28(16):. PubMed ID: 37630197
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trace water affects tris(pentafluorophenyl)borane catalytic activity in the Piers-Rubinsztajn reaction.
    Schneider AF; Chen Y; Brook MA
    Dalton Trans; 2019 Sep; 48(36):13599-13606. PubMed ID: 31455970
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Liquid triarylamines: the scope and limitations of Piers-Rubinsztajn conditions for obtaining triarylamine-siloxane hybrid materials.
    Kamino BA; Mills B; Reali C; Gretton MJ; Brook MA; Bender TP
    J Org Chem; 2012 Feb; 77(4):1663-74. PubMed ID: 22220839
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Siloxane-triarylamine hybrids: discrete room temperature liquid triarylamines via the Piers-Rubinsztajn reaction.
    Kamino BA; Grande JB; Brook MA; Bender TP
    Org Lett; 2011 Jan; 13(1):154-7. PubMed ID: 21128649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tris(pentafluorophenyl)borane-Catalyzed Reactions Using Silanes.
    Hackel T; McGrath NA
    Molecules; 2019 Jan; 24(3):. PubMed ID: 30691072
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Siloxane-Bond Formation Promoted by Lewis Acids: A Nonhydrolytic Sol-Gel Process and the Piers-Rubinsztajn Reaction.
    Wakabayashi R; Kuroda K
    Chempluschem; 2013 Aug; 78(8):764-774. PubMed ID: 31986688
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New Control Over Silicone Synthesis using SiH Chemistry: The Piers-Rubinsztajn Reaction.
    Brook MA
    Chemistry; 2018 Jun; 24(34):8458-8469. PubMed ID: 29468751
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tris(ortho-carboranyl)borane: An Isolable, Halogen-Free, Lewis Superacid.
    Akram MO; Tidwell JR; Dutton JL; Martin CD
    Angew Chem Int Ed Engl; 2022 Nov; 61(46):e202212073. PubMed ID: 36135949
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tris(pentafluorophenyl)borane and Beyond: Modern Advances in Borylation Chemistry.
    Lawson JR; Melen RL
    Inorg Chem; 2017 Aug; 56(15):8627-8643. PubMed ID: 28157303
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tris(pentafluorophenyl)borane catalyzed C-C and C-heteroatom bond formation.
    Kumar G; Roy S; Chatterjee I
    Org Biomol Chem; 2021 Feb; 19(6):1230-1267. PubMed ID: 33481983
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Twenty-five years of bis-pentafluorophenyl borane: a versatile reagent for catalyst and materials synthesis.
    Patrick EA; Piers WE
    Chem Commun (Camb); 2020 Jan; 56(6):841-853. PubMed ID: 31872836
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tris(pentafluorophenyl)borane: a special boron Lewis acid for special reactions.
    Erker G
    Dalton Trans; 2005 Jun; (11):1883-90. PubMed ID: 15909033
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Catalytic Synthesis of Oligosiloxanes Mediated by an Air Stable Catalyst, (C
    Rabanzo-Castillo KM; Kumar VB; Söhnel T; Leitao EM
    Front Chem; 2020; 8():477. PubMed ID: 32656180
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tris(pentafluorophenyl)borane as an efficient catalyst in the guanylation reaction of amines.
    Antiñolo A; Carrillo-Hermosilla F; Fernández-Galán R; Martínez-Ferrer J; Alonso-Moreno C; Bravo I; Moreno-Blázquez S; Salgado M; Villaseñor E; Albaladejo J
    Dalton Trans; 2016 Jun; 45(26):10717-29. PubMed ID: 27278089
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of structured polysiloxazanes via a Piers-Rubinsztajn reaction.
    Ai L; Chen Y; He L; Luo Y; Li S; Xu C
    Chem Commun (Camb); 2019 Nov; 55(93):14019-14022. PubMed ID: 31690921
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ring-Opening Polymerization of 1,3-Benzoxazines via Borane Catalyst.
    Arslan M; Kiskan B; Yagci Y
    Polymers (Basel); 2018 Feb; 10(3):. PubMed ID: 30966274
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Use of Piers-Rubinsztajn Chemistry to Access Unique and Challenging Silicon Phthalocyanines.
    Szawiola AM; Lessard BH; Raboui H; Bender TP
    ACS Omega; 2021 Oct; 6(41):26857-26869. PubMed ID: 34693107
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tris(pentafluorophenyl)borane-Catalyzed Formal Cyanoalkylation of Indoles with Cyanohydrins.
    Kiyokawa K; Urashima N; Minakata S
    J Org Chem; 2021 Jun; 86(12):8389-8401. PubMed ID: 34077225
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mechanistic insight into the catalytic hydrogenation of nonactivated aldehydes with a Hantzsch ester in the presence of a series of organoboranes: NMR and DFT studies.
    Hamasaka G; Tsuji H; Ehara M; Uozumi Y
    RSC Adv; 2019 Mar; 9(18):10201-10210. PubMed ID: 35520935
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.