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 *

190 related articles for article (PubMed ID: 24597715)

  • 1. Simple and catalyst-free synthesis of meso-O-, -S-, and -C-substituted porphyrins.
    Chen Q; Zhu YZ; Fan QJ; Zhang SC; Zheng JY
    Org Lett; 2014 Mar; 16(6):1590-3. PubMed ID: 24597715
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Catalyst-free aromatic nucleophilic substitution of meso-bromoporphyrins with azide anion: efficient synthesis and structural analyses of meso-azidoporphyrins.
    Yamashita K; Kataoka K; Asano MS; Sugiura K
    Org Lett; 2012 Jan; 14(1):190-3. PubMed ID: 22166089
    [TBL] [Abstract][Full Text] [Related]  

  • 3. From thioether substituted porphyrins to sulfur linked porphyrin dimers: an unusual SNAr via thiolate displacement?
    Ryan AA; Plunkett S; Casey A; McCabe T; Senge MO
    Chem Commun (Camb); 2014 Jan; 50(3):353-5. PubMed ID: 24247987
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Facile and efficient hypervalent iodine(III)-mediated meso-functionalization of porphyrins.
    Shen DM; Liu C; Chen XG; Chen QY
    J Org Chem; 2009 Jan; 74(1):206-11. PubMed ID: 19053580
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Direct arylation of meso-formyl porphyrin.
    Tokuji S; Awane H; Yorimitsu H; Osuka A
    Chemistry; 2013 Jan; 19(1):64-8. PubMed ID: 23255083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inexpensive and efficient Ullmann methodology to prepare donor-substituted porphyrins.
    Haumesser J; Pereira AM; Gisselbrecht JP; Merahi K; Choua S; Weiss J; Cavaleiro JA; Ruppert R
    Org Lett; 2013 Dec; 15(24):6282-5. PubMed ID: 24283676
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nucleophilic substitution as a tool for the synthesis of unsymmetrical porphyrins.
    Senge MO
    Acc Chem Res; 2005 Sep; 38(9):733-43. PubMed ID: 16171316
    [TBL] [Abstract][Full Text] [Related]  

  • 8. General synthesis of meso-amidoporphyrins via palladium-catalyzed amidation.
    Gao GY; Chen Y; Zhang XP
    Org Lett; 2004 May; 6(11):1837-40. PubMed ID: 15151427
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Peripherally Silylated Porphyrins.
    Kato K; Fujimoto K; Yorimitsu H; Osuka A
    Chemistry; 2015 Sep; 21(39):13522-5. PubMed ID: 26356498
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nucleophilic ring opening of meso-substituted 5-oxaporphyrin by oxygen, nitrogen, sulfur, and carbon nucleophiles.
    Kakeya K; Aozasa M; Mizutani T; Hitomi Y; Kodera M
    J Org Chem; 2014 Mar; 79(6):2591-600. PubMed ID: 24597593
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gram-scale synthesis of nickel(II) norcorrole: the smallest antiaromatic porphyrinoid.
    Ito T; Hayashi Y; Shimizu S; Shin JY; Kobayashi N; Shinokubo H
    Angew Chem Int Ed Engl; 2012 Aug; 51(34):8542-5. PubMed ID: 22811074
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Sn(IV)-porphyrin-based metal-organic framework for the selective photo-oxygenation of phenol and sulfides.
    Xie MH; Yang XL; Zou C; Wu CD
    Inorg Chem; 2011 Jun; 50(12):5318-20. PubMed ID: 21568275
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis and reactions of the first fluoroalkylated Ni(II) N-confused porphyrins.
    Jiang HW; Chen QY; Xiao JC; Gu YC
    Chem Commun (Camb); 2008 Nov; (42):5435-7. PubMed ID: 18985235
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Practical and efficient synthesis of various meso-functionalized porphyrins via simple ligand-free nickel-catalyzed C-O, C-N, and C-C cross-coupling reactions.
    Liu C; Shen DM; Chen QY
    J Org Chem; 2007 Apr; 72(8):2732-6. PubMed ID: 17348707
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthetic routes to meso-patterned porphyrins.
    Lindsey JS
    Acc Chem Res; 2010 Feb; 43(2):300-11. PubMed ID: 19863076
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of meso-arylsulfanyl- and alkylsulfanyl-substituted porphyrins via palladium-mediated C-S bond formation.
    Gao GY; Colvin AJ; Chen Y; Zhang XP
    J Org Chem; 2004 Dec; 69(25):8886-92. PubMed ID: 15575770
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ultrafast stimulated emission and structural dynamics in nickel porphyrins.
    Zhang X; Wasinger EC; Muresan AZ; Attenkofer K; Jennings G; Lindsey JS; Chen LX
    J Phys Chem A; 2007 Nov; 111(46):11736-42. PubMed ID: 17966996
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Aromatic nucleophilic substitution (S(N)Ar) of meso-nitroporphyrin with azide and amines as an alternative metal catalyst free synthetic approach to obtain meso-N-substituted porphyrins.
    Devillers CH; Hebié S; Lucas D; Cattey H; Clément S; Richeter S
    J Org Chem; 2014 Jul; 79(14):6424-34. PubMed ID: 24960068
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Insertion of Ni(I) into Porphyrins at Room Temperature: Preparation of Ni(II)porphyrins, and Ni(II)chlorins and Observation of Hydroporphyrin Intermediates.
    Peters MK; Herges R
    Inorg Chem; 2018 Mar; 57(6):3177-3182. PubMed ID: 29498852
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A general and efficient palladium-catalyzed intramolecular cyclization reaction of beta-brominated porphyrins.
    Shen DM; Liu C; Chen QY
    J Org Chem; 2006 Aug; 71(17):6508-11. PubMed ID: 16901136
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.