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 *

73 related articles for article (PubMed ID: 26107932)

  • 1. Leaving Group Effects on the Selectivity of the Silylation of Alcohols: The Reactivity-Selectivity Principle Revisited.
    Patschinski P; Zipse H
    Org Lett; 2015 Jul; 17(13):3318-21. PubMed ID: 26107932
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Lewis base-catalyzed silylation of alcohols--a mechanistic analysis.
    Patschinski P; Zhang C; Zipse H
    J Org Chem; 2014 Sep; 79(17):8348-57. PubMed ID: 25078902
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Substituent Effects in the Silylation of Secondary Alcohols: A Mechanistic Study.
    Marin-Luna M; Patschinski P; Zipse H
    Chemistry; 2018 Oct; 24(56):15052-15058. PubMed ID: 30070735
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cu(II)-ion-catalyzed solvolysis of N,N-bis(2-picolyl)ureas in alcohol solvents: evidence for cleavage involving nucleophilic addition and strong assistance of bis(2-picolyl)amine leaving group departure.
    Belzile MN; Neverov AA; Brown RS
    Inorg Chem; 2014 Aug; 53(15):7916-25. PubMed ID: 25054275
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An efficient protocol for alcohol protection under solvent- and catalyst-free conditions.
    Rao ChB; Chinnababu B; Venkateswarlu Y
    J Org Chem; 2009 Nov; 74(22):8856-8. PubMed ID: 19839567
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Catalytic Substrate-Selective Silylation of Primary Alcohols via Remote Functional-Group Discrimination.
    Hashimoto H; Ueda Y; Takasu K; Kawabata T
    Angew Chem Int Ed Engl; 2022 Apr; 61(18):e202114118. PubMed ID: 34942061
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Direct Amination of Alcohols Catalyzed by Aluminum Triflate: An Experimental and Computational Study.
    Payard PA; Gu Q; Guo W; Wang Q; Corbet M; Michel C; Sautet P; Grimaud L; Wischert R; Pera-Titus M
    Chemistry; 2018 Sep; 24(53):14146-14153. PubMed ID: 29882367
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Solvent polarity and organic reactivity in mixed solvents: evidence using a reactive molecular probe to assess the role of preferential solvation in aqueous alcohols.
    Bentley TW; Ebdon DN; Kim EJ; Koo IS
    J Org Chem; 2005 Mar; 70(5):1647-53. PubMed ID: 15730284
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ruthenium-catalyzed N-alkylation of amines with alcohols under mild conditions using the borrowing hydrogen methodology.
    Enyong AB; Moasser B
    J Org Chem; 2014 Aug; 79(16):7553-63. PubMed ID: 25007235
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unsuccessful attempts to add alcohols to transient 2-amino-2-siloxy-silenes - leading to a new benign route for base-free alcohol protection.
    Guliashvili T; Tibbelin J; Ryu J; Ottosson H
    Dalton Trans; 2010 Oct; 39(39):9379-85. PubMed ID: 20733993
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rhenium-catalyzed 1,3-isomerization of allylic alcohols: scope and chirality transfer.
    Morrill C; Beutner GL; Grubbs RH
    J Org Chem; 2006 Sep; 71(20):7813-25. PubMed ID: 16995691
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Silylation-based kinetic resolution of monofunctional secondary alcohols.
    Sheppard CI; Taylor JL; Wiskur SL
    Org Lett; 2011 Aug; 13(15):3794-7. PubMed ID: 21714486
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cu(II)-catalyzed allylic silylation of Morita-Baylis-Hillman alcohols via dual activation of Si-B bond and hydroxyl group.
    Xuan QQ; Zhong NJ; Ren CL; Liu L; Wang D; Chen YJ; Li CJ
    J Org Chem; 2013 Nov; 78(21):11076-81. PubMed ID: 24093603
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regioselective silylation of N-phthaloylchitosan with TBDMS and TBDPS groups.
    Binette A; Gagnon J
    Biomacromolecules; 2007 Jun; 8(6):1812-5. PubMed ID: 17487971
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cytochrome P-450 model reactions: efficient and highly selective oxidation of alcohols with tetrabutylammonium peroxymonosulfate catalyzed by Mn-porphyrins.
    Rezaeifard A; Jafarpour M; Moghaddam GK; Amini F
    Bioorg Med Chem; 2007 Apr; 15(8):3097-101. PubMed ID: 17293117
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Borylation and silylation of C-H bonds: a platform for diverse C-H bond functionalizations.
    Hartwig JF
    Acc Chem Res; 2012 Jun; 45(6):864-73. PubMed ID: 22075137
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A computational model relating structure and reactivity in enantioselective oxidations of secondary alcohols by (-)-sparteine-Pd(II) complexes.
    Nielsen RJ; Keith JM; Stoltz BM; Goddard WA
    J Am Chem Soc; 2004 Jun; 126(25):7967-74. PubMed ID: 15212546
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Facile nucleophilic fluorination reactions using tert-alcohols as a reaction medium: significantly enhanced reactivity of alkali metal fluorides and improved selectivity.
    Kim DW; Jeong HJ; Lim ST; Sohn MH; Katzenellenbogen JA; Chi DY
    J Org Chem; 2008 Feb; 73(3):957-62. PubMed ID: 18166063
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reactivity of alcohols toward the phosphoenzyme intermediate in the protein-tyrosine phosphatase-catalyzed reaction: probing the transition state of the dephosphorylation step.
    Zhao Y; Zhang ZY
    Biochemistry; 1996 Sep; 35(36):11797-804. PubMed ID: 8794761
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dynamic effects dictate the mechanism and selectivity of dehydration-rearrangement reactions of protonated alcohols [Me2 (R)CCH(OH2 )Me](+) (R=Me, Et, iPr) in the gas phase.
    de Souza MA; Ventura E; do Monte SA; Riveros JM; Longo RL
    Chemistry; 2014 Oct; 20(42):13742-54. PubMed ID: 25179304
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.