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 *

111 related articles for article (PubMed ID: 11853426)

  • 1. Asymmetric synthesis of 1-aryl-1,2-ethanediols from arylacetylenes by palladium-catalyzed asymmetric hydrosilylation as a key step.
    Shimada T; Mukaide K; Shinohara A; Han JW; Hayashi T
    J Am Chem Soc; 2002 Feb; 124(8):1584-5. PubMed ID: 11853426
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Asymmetric hydrosilylation of styrenes catalyzed by palladium-MOP complexes: ligand modification and mechanistic studies.
    Hayashi T; Hirate S; Kitayama K; Tsuji H; Torii A; Uozumi Y
    J Org Chem; 2001 Feb; 66(4):1441-9. PubMed ID: 11312978
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Asymmetric Hydrosilylation of β-Silyl Styrenes Catalyzed by a Chiral Palladium Complex.
    Wang YF; He YH; Su Y; Ji Y; Li R
    J Org Chem; 2022 Mar; 87(5):2831-2844. PubMed ID: 35080877
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis and application of bulky phosphoramidites: highly effective monophosphorus ligands for asymmetric hydrosilylation of styrenes.
    Zhang F; Fan QH
    Org Biomol Chem; 2009 Nov; 7(21):4470-4. PubMed ID: 19830297
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chiral bisphosphine BINAP-stabilized gold and palladium nanoparticles with small size and their palladium nanoparticle-catalyzed asymmetric reaction.
    Tamura M; Fujihara H
    J Am Chem Soc; 2003 Dec; 125(51):15742-3. PubMed ID: 14677954
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New Strategy for the Synthesis of Some Valuable Chiral 1,3-Diols with High Enantiomeric Purity: New Organocatalyst, Asymmetric Aldol Reaction, and Reduction.
    Yıldız T; Hasdemir B; Yaşa H; Başpınar Küçük H
    ACS Omega; 2024 Mar; 9(11):12657-12664. PubMed ID: 38524485
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A trifunctional catalyst for one-pot synthesis of chiral diols via Heck coupling-N-oxidation-asymmetric dihydroxylation: application for the synthesis of diltiazem and taxol side chain.
    Choudary BM; Chowdari NS; Madhi S; Kantam ML
    J Org Chem; 2003 Mar; 68(5):1736-46. PubMed ID: 12608786
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Palladium-catalyzed asymmetric silaboration of allenes.
    Ohmura T; Taniguchi H; Suginome M
    J Am Chem Soc; 2006 Oct; 128(42):13682-3. PubMed ID: 17044684
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cobalt-Catalyzed Regiodivergent Double Hydrosilylation of Arylacetylenes.
    Cheng Z; Li M; Zhang XY; Sun Y; Yu QL; Zhang XH; Lu Z
    Angew Chem Int Ed Engl; 2023 Jan; 62(1):e202215029. PubMed ID: 36330602
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stereoselective Hydrosilylation of 1,2-Diketones Catalyzed by Chiral Frustrated Lewis Pairs.
    Liu T; Meng W; Feng X; Du H
    Angew Chem Int Ed Engl; 2024 Jan; 63(5):e202313957. PubMed ID: 38065841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copper-Catalyzed Asymmetric Hydrosilylation of β-Nitroethyl Aryl Ketones.
    Zeng W; Tan X; Yu Y; Chen GQ; Zhang X
    Org Lett; 2020 Feb; 22(3):858-862. PubMed ID: 31916775
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis of Chiral Poly(silyl ether)s via CuH-Catalyzed Asymmetric Hydrosilylation Polymerization of Diketones with Silanes.
    Wang XQ; Zhai XY; Wu B; Bai YQ; Zhou YG
    ACS Macro Lett; 2020 Jul; 9(7):969-973. PubMed ID: 35648609
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cyclization of o-Allylstyrene via Hydrosilylation: Mechanistic Aspects of Hydrosilylation of Styrenes Catalyzed by Palladium-Phosphine Complexes.
    Uozumi Y; Tsuji H; Hayashi T
    J Org Chem; 1998 Sep; 63(18):6137-6140. PubMed ID: 11672242
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Asymmetric synthesis of axially chiral 1-aryl-5,6,7,8-tetrahydroquinolines by cobalt-catalyzed [2 + 2 + 2] cycloaddition reaction of 1-aryl-1,7-octadiynes and nitriles.
    Hapke M; Kral K; Fischer C; Spannenberg A; Gutnov A; Redkin D; Heller B
    J Org Chem; 2010 Jun; 75(12):3993-4003. PubMed ID: 20481604
    [TBL] [Abstract][Full Text] [Related]  

  • 15. N,N-Disubstituted Allylic Amine Type Aminophosphines with C(aryl)-N(amine) Bond Axial Chirality: Synthesis and Application to Palladium-Catalyzed Asymmetric Allylic Alkylation with Malonates.
    Mino T; Youda J; Ebisawa T; Shima Y; Nishikawa K; Yoshida Y; Sakamoto M
    J Oleo Sci; 2018 Oct; 67(10):1189-1199. PubMed ID: 30210075
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New air-stable planar chiral ferrocenyl monophosphine ligands: Suzuki cross-coupling of aryl chlorides and bromides.
    Jensen JF; Johannsen M
    Org Lett; 2003 Aug; 5(17):3025-8. PubMed ID: 12916972
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Asymmetric synthesis of functionalized 1,3-diphosphines via chiral palladium complex promoted hydrophosphination of activated olefins.
    Yuan M; Zhang N; Pullarkat SA; Li Y; Liu F; Pham PT; Leung PH
    Inorg Chem; 2010 Feb; 49(3):989-96. PubMed ID: 20041646
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new class of chiral P,N-ligands and their application in palladium-catalyzed asymmetric allylic substitution reactions.
    Lyle MP; Narine AA; Wilson PD
    J Org Chem; 2004 Jul; 69(15):5060-4. PubMed ID: 15255736
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Palladium-catalyzed enantioselective allylic alkylation of thiocarboxylate ions: asymmetric synthesis of allylic thioesters and memory effect/dynamic kinetic resolution of allylic esters.
    Lüssem BJ; Gais HJ
    J Org Chem; 2004 Jun; 69(12):4041-52. PubMed ID: 15176829
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An enantioselective, intermolecular α-arylation of ester enolates to form tertiary stereocenters.
    Huang Z; Liu Z; Zhou JS
    J Am Chem Soc; 2011 Oct; 133(40):15882-5. PubMed ID: 21910505
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.