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 *

409 related articles for article (PubMed ID: 19323574)

  • 1. Synthesis of 2-alkyl-substituted chromone derivatives using microwave irradiation.
    Fridén-Saxin M; Pemberton N; Andersson Kda S; Dyrager C; Friberg A; Grøtli M; Luthman K
    J Org Chem; 2009 Apr; 74(7):2755-9. PubMed ID: 19323574
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Base-promoted one-pot tandem reaction of 3-(1-alkynyl)chromones under microwave irradiation to functionalized amino-substituted xanthones.
    Liu Y; Huang L; Xie F; Hu Y
    J Org Chem; 2010 Sep; 75(18):6304-7. PubMed ID: 20738144
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of 2,3,6,8-tetrasubstituted chromone scaffolds.
    Dahlén K; Wallén EA; Grøtli M; Luthman K
    J Org Chem; 2006 Sep; 71(18):6863-71. PubMed ID: 16930039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Efficient synthesis of imidazoles from aldehydes and 1,2-diketones using microwave irradiation.
    Wolkenberg SE; Wisnoski DD; Leister WH; Wang Y; Zhao Z; Lindsley CW
    Org Lett; 2004 Apr; 6(9):1453-6. PubMed ID: 15101765
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microwave-assisted combinatorial synthesis of hexa-substituted 1,4-dihydropyridines scaffolds using one-pot two-step multicomponent reaction followed by a S-alkylation.
    Li M; Zuo Z; Wen L; Wang S
    J Comb Chem; 2008; 10(3):436-41. PubMed ID: 18412399
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reactions of 3-isochromanone with aromatic aldehydes--microwave assisted condensations performed on solid basic inorganic supports.
    Vass A; Földesi A; Lóránd T
    J Biochem Biophys Methods; 2006 Nov; 69(1-2):179-87. PubMed ID: 16678272
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Efficient synthesis of chromone and flavonoid derivatives with diverse heterocyclic units.
    Arai MA; Sato M; Sawada K; Hosoya T; Ishibashi M
    Chem Asian J; 2008 Dec; 3(12):2056-64. PubMed ID: 18830978
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Stereoselective synthesis of novel highly substituted isochromanone and isoquinolinone-containing exocyclic tetrasubstituted alkenes.
    Arthuis M; Pontikis R; Florent JC
    J Org Chem; 2009 Mar; 74(5):2234-7. PubMed ID: 19199667
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new mild base-catalyzed Mannich reaction of hetero-arylamines in water: highly efficient stereoselective synthesis of beta-aminoketones under microwave heating.
    Hao WJ; Jiang B; Tu SJ; Cao XD; Wu SS; Yan S; Zhang XH; Han ZG; Shi F
    Org Biomol Chem; 2009 Apr; 7(7):1410-4. PubMed ID: 19300827
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Iron-catalyzed, microwave-promoted, one-pot synthesis of 9-substituted xanthenes by a cascade benzylation-cyclization process.
    Xu X; Xu X; Li H; Xie X; Li Y
    Org Lett; 2010 Jan; 12(1):100-3. PubMed ID: 19938841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microwave promoted C6-alkylation of purines through S(N)Ar-based reaction of 6-chloropurines with 3-alkyl-acetylacetone.
    Guo HM; Zhang Y; Niu HY; Wang DC; Chu ZL; Qu GR
    Org Biomol Chem; 2011 Apr; 9(7):2065-8. PubMed ID: 21340084
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multicomponent, one-pot sequential synthesis of 1,3,5- and 1,3,5,5-substituted barbiturates.
    Volonterio A; Zanda M
    J Org Chem; 2008 Oct; 73(19):7486-97. PubMed ID: 18754580
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rhodium catalyzed oxidative coupling of salicylaldehydes with diazabicyclic olefins: a one pot strategy involving aldehyde C-H cleavage and π-allyl chemistry towards the synthesis of fused ring chromanones.
    Jijy E; Prakash P; Shimi M; Pihko PM; Joseph N; Radhakrishnan KV
    Chem Commun (Camb); 2013 Aug; 49(66):7349-51. PubMed ID: 23846351
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Novel Synthesis of Highly Functionalized Pyridines by a One-Pot, Three-Component Tandem Reaction of Aldehydes, Malononitrile and N-Alkyl-2-cyanoacetamides under Microwave Irradiation.
    Mekheimer RA; Al-Sheikh MA; Medrasi HY; Alsofyani NHH
    Molecules; 2018 Mar; 23(3):. PubMed ID: 29522435
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A general approach to high-yielding asymmetric synthesis of chiral 3-alkyl-4-nitromethylchromans via cascade Barbas-Michael and acetalization reactions.
    Ramachary DB; Prasad MS; Madhavachary R
    Org Biomol Chem; 2011 Apr; 9(8):2715-21. PubMed ID: 21369625
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Facile synthesis of highly substituted 3-aminofurans from thiazolium salts, aldehydes, and dimethyl acetylenedicarboxylate.
    Ma C; Ding H; Wu G; Yang Y
    J Org Chem; 2005 Oct; 70(22):8919-23. PubMed ID: 16238328
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis and NMR studies of novel chromone-2-carboxamide derivatives.
    Gaspar A; Cagide F; Quezada E; Reis J; Uriarte E; Borges F
    Magn Reson Chem; 2013 Apr; 51(4):251-4. PubMed ID: 23408556
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Efficient construction of a 3C-xanthone-linked 3C-chromone scaffold by novel double Michael additions and cyclizations.
    Xie F; Chen H; Hu Y
    Org Lett; 2010 Jul; 12(13):3086-9. PubMed ID: 20533853
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Access to flavones via a microwave-assisted, one-pot Sonogashira-carbonylation-annulation reaction.
    Awuah E; Capretta A
    Org Lett; 2009 Aug; 11(15):3210-3. PubMed ID: 19580257
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Yb(OTf)3-catalyzed reactions of 5-alkylidene Meldrum's acids with phenols: one-pot assembly of 3,4-dihydrocoumarins, 4-chromanones, coumarins, and chromones.
    Fillion E; Dumas AM; Kuropatwa BA; Malhotra NR; Sitler TC
    J Org Chem; 2006 Jan; 71(1):409-12. PubMed ID: 16388672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.