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 *

107 related articles for article (PubMed ID: 37800444)

  • 1. Bifunctional thiourea-based organocatalyst promoted kinetic resolution polymerization of racemic lactide to isotactic polylactide.
    Dai J; Xiong W; Li DY; Cai Z; Zhu JB
    Chem Commun (Camb); 2023 Oct; 59(85):12731-12734. PubMed ID: 37800444
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isoselective Ring-Opening Polymerization of
    Orhan B; Tschan MJ; Wirotius AL; Dove AP; Coulembier O; Taton D
    ACS Macro Lett; 2018 Dec; 7(12):1413-1419. PubMed ID: 35651230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A chiral thiourea and a phosphazene for fast and stereoselective organocatalytic ring-opening-polymerization of racemic lactide.
    Zaky MS; Wirotius AL; Coulembier O; Guichard G; Taton D
    Chem Commun (Camb); 2021 Apr; 57(31):3777-3780. PubMed ID: 33734228
    [TBL] [Abstract][Full Text] [Related]  

  • 4. In-situ formation of biodegradable hydrogels by stereocomplexation of PEG-(PLLA)8 and PEG-(PDLA)8 star block copolymers.
    Hiemstra C; Zhong Z; Li L; Dijkstra PJ; Feijen J
    Biomacromolecules; 2006 Oct; 7(10):2790-5. PubMed ID: 17025354
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Reaching High Stereoselectivity and Activity in Organocatalyzed Ring-Opening Polymerization of Racemic Lactide by the Combined Use of a Chiral (Thio)Urea and a
    Zaky MS; Wirotius AL; Coulembier O; Guichard G; Taton D
    ACS Macro Lett; 2022 Sep; 11(9):1148-1155. PubMed ID: 36067070
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Stereoselective Ring-Opening Polymerization of
    Liu S; Li H; Zhao N; Li Z
    ACS Macro Lett; 2018 Jun; 7(6):624-628. PubMed ID: 35632967
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Highly Active Organocatalysts for Stereoselective Ring-Opening Polymerization of Racemic Lactide at Room Temperature.
    Liu Y; Zhang J; Kou X; Liu S; Li Z
    ACS Macro Lett; 2022 Oct; 11(10):1183-1189. PubMed ID: 36102870
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chiral 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD)-Catalyzed Stereoselective Ring-Opening Polymerization of
    Mahmood Q; Xu G; Zhou L; Guo X; Wang Q
    Polymers (Basel); 2020 Oct; 12(10):. PubMed ID: 33076378
    [TBL] [Abstract][Full Text] [Related]  

  • 9. From meso-Lactide to Isotactic Polylactide: Epimerization by B/N Lewis Pairs and Kinetic Resolution by Organic Catalysts.
    Zhu JB; Chen EY
    J Am Chem Soc; 2015 Oct; 137(39):12506-9. PubMed ID: 26388298
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alkaline Earth Metal-Mediated Highly Iso-selective Ring-Opening Polymerization of rac-Lactide.
    Bhattacharjee J; Harinath A; Sarkar A; Panda TK
    Chem Asian J; 2020 Mar; 15(6):860-866. PubMed ID: 32022475
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Catalyst-Sidearm-Induced Stereoselectivity Switching in Polymerization of a Racemic Lactone for Stereocomplexed Crystalline Polymer with a Circular Life Cycle.
    Zhu JB; Chen EY
    Angew Chem Int Ed Engl; 2019 Jan; 58(4):1178-1182. PubMed ID: 30501004
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Controlled and stereoselective polymerization of lactide: kinetics, selectivity, and microstructures.
    Zhong Z; Dijkstra PJ; Feijen J
    J Am Chem Soc; 2003 Sep; 125(37):11291-8. PubMed ID: 16220951
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stereocontrolled polymerization of racemic lactide with chiral initiator: combining stereoelection and chiral ligand-exchange mechanism.
    Majerska K; Duda A
    J Am Chem Soc; 2004 Feb; 126(4):1026-7. PubMed ID: 14746463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Zinc complexes containing asymmetrical N,N,O-tridentate ligands and their application in lactide polymerization.
    Gao B; Duan R; Pang X; Li X; Qu Z; Shao H; Wang X; Chen X
    Dalton Trans; 2013 Dec; 42(46):16334-42. PubMed ID: 24065120
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Effect of Stereocomplex Polylactide Particles on the Stereocomplexation of High Molecular Weight Polylactide Blends.
    Samsuri M; Iswaldi I; Purnama P
    Polymers (Basel); 2021 Jun; 13(12):. PubMed ID: 34205488
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mechanistic Insight into the Stereochemical Control of Lactide Polymerization by Salan-Aluminum Catalysts.
    Press K; Goldberg I; Kol M
    Angew Chem Int Ed Engl; 2015 Dec; 54(49):14858-61. PubMed ID: 25981978
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Dual-Stereocontrol Mechanism: Heteroselective Polymerization of rac-Lactide and Syndioselective Polymerization of meso-Lactide by Chiral Aluminum Salan Catalysts.
    Hador R; Botta A; Venditto V; Lipstman S; Goldberg I; Kol M
    Angew Chem Int Ed Engl; 2019 Oct; 58(41):14679-14685. PubMed ID: 31355508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Properties Enhancement of High Molecular Weight Polylactide Using Stereocomplex Polylactide as a Nucleating Agent.
    Purnama P; Samsuri M; Iswaldi I
    Polymers (Basel); 2021 May; 13(11):. PubMed ID: 34070263
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Determination of Polylactide Microstructure by Homonuclear Decoupled
    Singha Roy S; Sarkar S; Chakraborty D
    Chem Rec; 2021 Aug; 21(8):1968-1984. PubMed ID: 34327819
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Desymmetrization and Kinetic Resolution of Endoperoxides Using a Bifunctional Organocatalyst.
    Legendre SVA; Sumby CJ; Karton A; Greatrex BW
    J Org Chem; 2023 Aug; 88(16):11444-11449. PubMed ID: 37552803
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.