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Journal Abstract Search

196 related items for PubMed ID: 31336669

  • 1. Synthesis of the Core Framework of the Cornexistins by Intramolecular Nozaki-Hiyama-Kishi Coupling.
    Aimon A, Farrugia LJ, Clark JS.
    Molecules; 2019 Jul 22; 24(14):. PubMed ID: 31336669
    [Abstract] [Full Text] [Related]

  • 2. Synthesis of the carbocyclic core of the cornexistins by ring-closing metathesis.
    Clark JS, Marlin F, Nay B, Wilson C.
    Org Lett; 2003 Jan 09; 5(1):89-92. PubMed ID: 12509898
    [Abstract] [Full Text] [Related]

  • 3. Role of the Nozaki-Hiyama-Takai-Kishi Reaction in the Synthesis of Natural Products.
    Gil A, Albericio F, Álvarez M.
    Chem Rev; 2017 Jun 28; 117(12):8420-8446. PubMed ID: 28627170
    [Abstract] [Full Text] [Related]

  • 4. Evolution of a Strategy for the Total Synthesis of (+)-Cornexistin.
    Wildermuth RE, Steinborn C, Barber DM, Mühlfenzl KS, Kendlbacher M, Mayer P, Wurst K, Magauer T.
    Chemistry; 2021 Aug 19; 27(47):12181-12189. PubMed ID: 34105834
    [Abstract] [Full Text] [Related]

  • 5. Total Synthesis of (+)-Cornexistin.
    Steinborn C, Wildermuth RE, Barber DM, Magauer T.
    Angew Chem Int Ed Engl; 2020 Sep 21; 59(39):17282-17285. PubMed ID: 32558114
    [Abstract] [Full Text] [Related]

  • 6. Synthetic studies on the cornexistins: synthesis of (+/-)-5-epi-hydroxycornexistin.
    Clark JS, Northall JM, Marlin F, Nay B, Wilson C, Blake AJ, Waring MJ.
    Org Biomol Chem; 2008 Nov 07; 6(21):4012-25. PubMed ID: 18931810
    [Abstract] [Full Text] [Related]

  • 7. Investigations into Simplified Analogues of the Herbicidal Natural Product (+)-Cornexistin.
    Steinborn C, Tancredi A, Habiger C, Diederich C, Kramer J, Reingruber AM, Laber B, Freigang J, Lange G, Schmutzler D, Machettira A, Besong G, Magauer T, Barber DM.
    Chemistry; 2023 Jul 11; 29(39):e202300199. PubMed ID: 36807428
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  • 13. Total synthesis of the antitumor acetogenin mosin B: desymmetrization approach to the stereodivergent synthesis of threo/trans/erythro-type acetogenins.
    Maezaki N, Kojima N, Sakamoto A, Tominaga H, Iwata C, Tanaka T, Monden M, Damdinsuren B, Nakamori S.
    Chemistry; 2003 Jan 20; 9(2):389-99. PubMed ID: 12532287
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  • 15. Natural product inspired design of enediyne prodrugs via rearrangement of an allylic double bond.
    Dai WM.
    Curr Med Chem; 2003 Nov 20; 10(21):2265-83. PubMed ID: 14529342
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  • 16. Collective Synthesis of Highly Oxygenated (Furano)germacranolides Derived from Elephantopus mollis and Elephantopus tomentosus.
    Patouret R, Cham N, Chiba S.
    Angew Chem Int Ed Engl; 2024 May 06; 63(19):e202402050. PubMed ID: 38488804
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  • 17. Synthesis of the C1-C21 domain of azaspiracids-1 and -3.
    Zhang Z, Ding Y, Xu J, Chen Y, Forsyth CJ.
    Org Lett; 2013 May 17; 15(10):2338-41. PubMed ID: 23627769
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  • 18. Total Synthesis of Isoxeniolide A.
    Betschart L, Altmann KH.
    Angew Chem Int Ed Engl; 2024 Feb 26; 63(9):e202315423. PubMed ID: 38118052
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  • 19. Synthesis of the C1-C26 hexacyclic subunit of pectenotoxin 2.
    Kubo O, Canterbury DP, Micalizio GC.
    Org Lett; 2012 Nov 16; 14(22):5748-51. PubMed ID: 23101680
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  • 20. Total Syntheses of Strasseriolide A and B, Antimalarial Macrolide Natural Products.
    Salituro LJ, Pazienza JE, Rychnovsky SD.
    Org Lett; 2022 Feb 11; 24(5):1190-1194. PubMed ID: 35094508
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