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 *

153 related articles for article (PubMed ID: 35529638)

  • 1. Microwave-assisted iodine-catalyzed oxidative coupling of dibenzyl(difurfuryl)disulfides with amines: a rapid and efficient protocol for thioamides.
    Chen J; Mei L; Liu J; Zhong C; Yuan B; Li Q
    RSC Adv; 2019 Sep; 9(49):28576-28580. PubMed ID: 35529638
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oxidative coupling of dibenzyl disulfide with amines catalyzed by quinoline-bromine complex: access to thioamides.
    Rezapour M; Abbasi M
    Mol Divers; 2023 Feb; 27(1):159-165. PubMed ID: 35294672
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of thioamides via one-pot A(3)-coupling of alkynyl bromides, amines, and sodium sulfide.
    Sun Y; Jiang H; Wu W; Zeng W; Li J
    Org Biomol Chem; 2014 Jan; 12(4):700-7. PubMed ID: 24306511
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Efficient and selective multicomponent oxidative coupling of two different aliphatic primary amines into thioamides by elemental sulfur.
    Nguyen TB; Ermolenko L; Al-Mourabit A
    Org Lett; 2012 Aug; 14(16):4274-7. PubMed ID: 22862830
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microwave-Assisted Cu(I)-Catalyzed Synthesis of Unsymmetrical 1,4-Diamino-2-butynes via Cross-A
    Xu X; Feng H; Van der Eycken EV
    J Org Chem; 2021 Oct; 86(20):14036-14043. PubMed ID: 33890472
    [TBL] [Abstract][Full Text] [Related]  

  • 6. One-pot synthesis of 3,5-disubstituted 1,2,4-thiadiazoles from nitriles and thioamides via I
    Chai L; Xu Y; Ding T; Fang X; Zhang W; Wang Y; Lu M; Xu H; Yang X
    Org Biomol Chem; 2017 Oct; 15(39):8410-8417. PubMed ID: 28952634
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hypervalent iodine-promoted twofold oxidative coupling of amines with amides and thioamides: chemoselective pathway to oxazoles and thiazoles.
    Nan J; Ren X; Yan Q; Liu S; Wang J; Ma Y; Szostak M
    Chem Sci; 2023 Mar; 14(12):3338-3345. PubMed ID: 36970078
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis of 2-azaindolizines by using an iodine-mediated oxidative desulfurization promoted cyclization of N-2-pyridylmethyl thioamides and an investigation of their photophysical properties.
    Shibahara F; Kitagawa A; Yamaguchi E; Murai T
    Org Lett; 2006 Nov; 8(24):5621-4. PubMed ID: 17107087
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Enaminones via ruthenium-catalyzed coupling of thioamides and α-diazocarbonyl compounds.
    Koduri ND; Wang Z; Cannell G; Cooley K; Lemma TM; Miao K; Nguyen M; Frohock B; Castaneda M; Scott H; Albinescu D; Hussaini SR
    J Org Chem; 2014 Aug; 79(16):7405-14. PubMed ID: 25058113
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Palladium(0)-catalyzed, copper(I)-mediated coupling of boronic acids with cyclic thioamides. selective carbon-carbon bond formation for the functionalization of heterocycles.
    Prokopcová H; Kappe CO
    J Org Chem; 2007 Jun; 72(12):4440-8. PubMed ID: 17497803
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Direct Transamidation of Thioamides with Amines via Acetophenone-Promoted Enamine Catalysis under Metal-Free Conditions.
    Tan Y; Ni P; Jiang WJ; Fu Y; Ding Q
    J Org Chem; 2024 Mar; 89(5):2939-2950. PubMed ID: 38381084
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Direct synthesis of polysubstituted 2-aminothiophenes by Cu(II)-catalyzed addition/oxidative cyclization of alkynoates with thioamides.
    Ge LS; Wang ZL; An XL; Luo X; Deng WP
    Org Biomol Chem; 2014 Nov; 12(42):8473-9. PubMed ID: 25227952
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copper(i) chloride promoted Csp(2)-N cross-coupling of 1,2-di(pyrimidin-2-yl) disulfides with amines: an efficient approach to obtain C2-amino functionalized pyrimidines.
    Wei KJ; Quan ZJ; Zhang Z; Da YX; Wang XC
    Org Biomol Chem; 2016 Feb; 14(8):2395-8. PubMed ID: 26821885
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microwave-Assisted Copper-Catalyzed Oxidative Cyclization of Acrylamides with Non-Activated Ketones.
    Zhao Y; Sharma N; Sharma UK; Li Z; Song G; Van der Eycken EV
    Chemistry; 2016 Apr; 22(17):5878-82. PubMed ID: 26868308
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An efficient and straightforward approach for accessing thionoesters
    Liu Y; Mo X; Majeed I; Zhang M; Wang H; Zeng Z
    Org Biomol Chem; 2022 Feb; 20(7):1532-1537. PubMed ID: 35129563
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of α-amino amidines through molecular iodine-catalyzed three-component coupling of isocyanides, aldehydes and amines.
    Adiyala PR; Chandrasekhar D; Kapure JS; Reddy CN; Maurya RA
    Beilstein J Org Chem; 2014; 10():2065-70. PubMed ID: 25246965
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An oxidative cross-coupling reaction of 4-hydroxydithiocoumarin and amines/thiols using a combination of I
    Mahato K; Arora N; Ray Bagdi P; Gattu R; Ghosh SS; Khan AT
    Chem Commun (Camb); 2018 Feb; 54(12):1513-1516. PubMed ID: 29364291
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis of Nitriles via the Iodine-Mediated Dehydrosulfurization of Thioamides.
    Murata Y; Iwasa H; Matsumura M; Yasuike S
    Chem Pharm Bull (Tokyo); 2020; 68(7):679-681. PubMed ID: 32612004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Selectfluor-promoted oxidative reaction of disulfides and amines: access to sulfinamides.
    Mei H; Liu J; Pajkert R; Röschenthaler GV; Han J
    Org Biomol Chem; 2020 May; 18(19):3761-3766. PubMed ID: 32373830
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Efficient preparation of unsymmetrical disulfides by nickel-catalyzed reductive coupling strategy.
    Wang F; Chen Y; Rao W; Ackermann L; Wang SY
    Nat Commun; 2022 May; 13(1):2588. PubMed ID: 35546155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.