BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 30028625)

  • 1. Catalytic Asymmetric Total Syntheses of Naturally Occurring Amarylidaceae Alkaloids, (-)-Crinine, (-)- epi-Crinine, (-)-Oxocrinine, (+)- epi-Elwesine, (+)-Vittatine, and (+)- epi-Vittatine.
    Das MK; Kumar N; Bisai A
    Org Lett; 2018 Aug; 20(15):4421-4424. PubMed ID: 30028625
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enantioselective synthesis of Amaryllidaceae alkaloids (+)-vittatine, (+)-epi-vittatine, and (+)-buphanisine.
    Wei MX; Wang CT; Du JY; Qu H; Yin PR; Bao X; Ma XY; Zhao XH; Zhang GB; Fan CA
    Chem Asian J; 2013 Sep; 8(9):1966-71. PubMed ID: 23788411
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chiral Bisphosphine-Catalyzed Asymmetric Staudinger/aza-Wittig Reaction: An Enantioselective Desymmetrizing Approach to Crinine-Type
    Yang H; Zhang J; Zhang S; Xue Z; Hu S; Chen Y; Tang Y
    J Am Chem Soc; 2024 May; 146(20):14136-14148. PubMed ID: 38642063
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Catalytic enantioselective and divergent total synthesis of (+)-10-oxocylindrocarpidine, (+)-cylindrocarpidine, (-)-N-acetylcylindrocarpinol, and (+)-aspidospermine.
    Shen XL; Zhao RR; Mo MJ; Peng FZ; Zhang HB; Shao ZH
    J Org Chem; 2014 Mar; 79(6):2473-80. PubMed ID: 24559389
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Base-catalyzed intramolecular hydroamination of cyclohexa-2,5-dienes: insights into the mechanism through DFT calculations and application to the total synthesis of epi-elwesine.
    Rousseau G; Lebeuf R; Schenk K; Castet F; Robert F; Landais Y
    Chemistry; 2014 Nov; 20(45):14771-82. PubMed ID: 25223607
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis of Amaryllidaceae Constituents and Unnatural Derivatives.
    Ghavre M; Froese J; Pour M; Hudlicky T
    Angew Chem Int Ed Engl; 2016 May; 55(19):5642-91. PubMed ID: 26969844
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new entry to Amaryllidaceae alkaloids from carbohydrates: total synthesis of (+)-vittatine.
    Bohno M; Imase H; Chida N
    Chem Commun (Camb); 2004 May; (9):1086-7. PubMed ID: 15116197
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The First Enantioselective Total Synthesis of (-)-trans-Dihydronarciclasine.
    Varró G; Hegedűs L; Simon A; Balogh A; Grün A; Leveles I; Vértessy BG; Kádas I
    J Nat Prod; 2017 Jun; 80(6):1909-1917. PubMed ID: 28581297
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Palladium-catalyzed asymmetric allylic substitution of 2-arylcyclohexenol derivatives: asymmetric total syntheses of (+)-crinamine, (-)-haemanthidine, and (+)-pretazettine.
    Nishimata T; Sato Y; Mori M
    J Org Chem; 2004 Mar; 69(6):1837-43. PubMed ID: 15058926
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Total syntheses of (+/-)-crinine, (+/-)-crinamine, and (+/-)-6a-epi-crinamine via the regioselective synthesis and Diels-Alder reaction of 3-aryl-5-bromo-2-pyrone.
    Nguyen TT; Chang J; Jung EJ; Cho CG
    J Org Chem; 2008 Aug; 73(16):6258-64. PubMed ID: 18630885
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mini-review of the anti-SARS-CoV-2 potency of Amaryllidaceae alkaloids.
    Le NT; Janssen K; Kirchmair J; Pieters L; Tuenter E
    Phytomedicine; 2024 Jul; 129():155576. PubMed ID: 38579643
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Catalytic Asymmetric Total Syntheses of (-)-Galanthamine and (-)-Lycoramine.
    Zhang Q; Zhang FM; Zhang CS; Liu SZ; Tian JM; Wang SH; Zhang XM; Tu YQ
    J Org Chem; 2019 Oct; 84(19):12664-12671. PubMed ID: 31498620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stereoselective synthesis of 7-epi-incarvilline.
    Seo H; Yun H; Lee S; Jang J; Han YT; Kim DD; Lee J; Suh YG
    Org Lett; 2013 Feb; 15(3):531-3. PubMed ID: 23343424
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Total synthesis and biological evaluation of Amaryllidaceae alkaloids: narciclasine, ent-7-deoxypancratistatin, regioisomer of 7-deoxypancratistatin, 10b-epi-deoxypancratistatin, and truncated derivatives.
    Hudlicky T; Rinner U; Gonzalez D; Akgun H; Schilling S; Siengalewicz P; Martinot TA; Pettit GR
    J Org Chem; 2002 Dec; 67(25):8726-43. PubMed ID: 12467383
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gigantelline, gigantellinine and gigancrinine, cherylline- and crinine-type alkaloids isolated from Crinum jagus with anti-acetylcholinesterase activity.
    Ka S; Masi M; Merindol N; Di Lecce R; Plourde MB; Seck M; Górecki M; Pescitelli G; Desgagne-Penix I; Evidente A
    Phytochemistry; 2020 Jul; 175():112390. PubMed ID: 32335411
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Crinine-type alkaloids from Hippeastrum aulicum and H. calyptratum.
    de Andrade JP; Guo Y; Font-Bardia M; Calvet T; Dutilh J; Viladomat F; Codina C; Nair JJ; Zuanazzi JAS; Bastida J
    Phytochemistry; 2014 Jul; 103():188-195. PubMed ID: 24768284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Catalytic asymmetric total synthesis of (-)-galanthamine and (-)-lycoramine.
    Li L; Yang Q; Wang Y; Jia Y
    Angew Chem Int Ed Engl; 2015 May; 54(21):6255-9. PubMed ID: 25847447
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A General Electro-Synthesis Approach to Amaryllidaceae Alkaloids.
    Pollok D; Großmann LM; Behrendt T; Opatz T; Waldvogel SR
    Chemistry; 2022 Sep; 28(50):e202201523. PubMed ID: 35662286
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A General, Concise Strategy that Enables Collective Total Syntheses of over 50 Protoberberine and Five Aporhoeadane Alkaloids within Four to Eight Steps.
    Zhou S; Tong R
    Chemistry; 2016 May; 22(21):7084-9. PubMed ID: 26990887
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chemoenzymatic approaches to lycorine-type Amaryllidaceae alkaloids: total syntheses of ent-lycoricidine, 3-epi-ent-lycoricidine, and 4-deoxy-3-epi-ent-lycoricidine.
    Matveenko M; Kokas OJ; Banwell MG; Willis AC
    Org Lett; 2007 Aug; 9(18):3683-5. PubMed ID: 17685535
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.