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 *

103 related articles for article (PubMed ID: 12375954)

  • 1. Toward a computational tool predicting the stereochemical outcome of asymmetric reactions. 1. Application to Sharpless asymmetric dihydroxylation.
    Moitessier N; Henry C; Len C; Chapleur Y
    J Org Chem; 2002 Oct; 67(21):7275-82. PubMed ID: 12375954
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review.
    Mushtaq A; Zahoor AF; Bilal M; Hussain SM; Irfan M; Akhtar R; Irfan A; Kotwica-Mojzych K; Mojzych M
    Molecules; 2023 Mar; 28(6):. PubMed ID: 36985698
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Toward a computational tool predicting the stereochemical outcome of asymmetric reactions: development of the molecular mechanics-based program ACE and application to asymmetric epoxidation reactions.
    Weill N; Corbeil CR; De Schutter JW; Moitessier N
    J Comput Chem; 2011 Oct; 32(13):2878-89. PubMed ID: 21735450
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Asymmetric synthesis of cyclic hydroxy ketones derived from enol ethers via sharpless asymmetric dihydroxylation. A study in the correlation of the enol ether chain length and enantioselectivity.
    Marcune BF; Karady S; Reider PJ; Miller RA; Biba M; DiMichele L; Reamer RA
    J Org Chem; 2003 Oct; 68(21):8088-91. PubMed ID: 14535787
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chemical and Electrochemical Asymmetric Dihydroxylation of Olefins in I(2)-K(2)CO(3)-K(2)OsO(2)(OH)(4) and I(2)-K(3)PO(4)/K(2)HPO(4)-K(2)OsO(2)(OH)(4) Systems with Sharpless' Ligand.
    Torii S; Liu P; Bhuvaneswari N; Amatore C; Jutand A
    J Org Chem; 1996 May; 61(9):3055-3060. PubMed ID: 11667167
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sodium chlorite as an efficient oxidant and hydroxy ion pump in osmium-catalyzed asymmetric dihydroxylation.
    Junttila MH; Hormi OE
    J Org Chem; 2004 Jul; 69(14):4816-20. PubMed ID: 15230608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Studies directed toward the exploitation of vicinal diols in the synthesis of (+)-nebivolol intermediates.
    Devi R; Das SK
    Beilstein J Org Chem; 2017; 13():571-578. PubMed ID: 28405237
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methanesulfonamide: a cosolvent and a general acid catalyst in sharpless asymmetric dihydroxylations.
    Junttila MH; Hormi OO
    J Org Chem; 2009 Apr; 74(8):3038-47. PubMed ID: 19301884
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The tethered aminohydroxylation (TA) reaction.
    Donohoe TJ; Johnson PD; Pye RJ
    Org Biomol Chem; 2003 Jun; 1(12):2025-8. PubMed ID: 12945888
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synthesis of Tuckolide, a New Cholesterol Biosynthesis Inhibitor.
    Andrus MB; Shih TL
    J Org Chem; 1996 Dec; 61(25):8780-8785. PubMed ID: 11667854
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Updating the asymmetric osmium-catalyzed dihydroxylation (AD) mnemonic: Q2MM modeling and new kinetic measurements.
    Fristrup P; Tanner D; Norrby PO
    Chirality; 2003 May; 15(4):360-8. PubMed ID: 12666245
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Temporary Protection of
    Coudray L; Montchamp JL
    European J Org Chem; 2009 Sep; 2009(27):. PubMed ID: 24273443
    [No Abstract]   [Full Text] [Related]  

  • 14. Asymmetric synthesis of biologically useful 3,4-disubstitutedgamma- lactone (3,4-db).
    Cheong CS; Park YJ; Lee SH; Im DS; Jung SH
    Enantiomer; 2000 Dec; 5(6):585-90. PubMed ID: 11342294
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Polymer enzyme conjugates as chiral ligands for sharpless dihydroxylation of alkenes in organic solvents.
    Konieczny S; Leurs M; Tiller JC
    Chembiochem; 2015 Jan; 16(1):83-90. PubMed ID: 25421303
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Substrate Directed Asymmetric Reactions.
    Bhadra S; Yamamoto H
    Chem Rev; 2018 Apr; 118(7):3391-3446. PubMed ID: 29570284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Asymmetric dihydroxylations of 1-substituted (E)- and (Z)-3-methylpent-2-en-4-ynes: full compliance with the Sharpless mnemonic re-established and embellished.
    Burghart-Stoll H; Böhnke O; Brückner R
    Org Lett; 2011 Mar; 13(5):1020-3. PubMed ID: 21271732
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Asymmetric synthesis of
    Konishi S; Ogura Y; Takikawa H; Watanabe H
    Biosci Biotechnol Biochem; 2020 Jan; 84(1):37-42. PubMed ID: 31578944
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Concise and Highly Enantioselective Total Synthesis of (+)-anti- and (-)-syn-Mefloquine Hydrochloride: Definitive Absolute Stereochemical Assignment of the Mefloquines.
    Rastelli EJ; Coltart DM
    Angew Chem Int Ed Engl; 2015 Nov; 54(47):14070-4. PubMed ID: 26422780
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A highly stereoselective synthesis of C-24 and C-25 oxysterols from desmosterol.
    Zhao Q; Qian C; Chen XZ
    Steroids; 2016 May; 109():16-21. PubMed ID: 26968128
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.