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 *

135 related articles for article (PubMed ID: 33215181)

  • 1. Deep eutectic solvent-catalyzed Meyer-Schuster rearrangement of propargylic alcohols under mild and bench reaction conditions.
    Ríos-Lombardía N; Cicco L; Yamamoto K; Hernández-Fernández JA; Morís F; Capriati V; García-Álvarez J; González-Sabín J
    Chem Commun (Camb); 2020 Dec; 56(96):15165-15168. PubMed ID: 33215181
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Metal-catalyzed transformations of propargylic alcohols into alpha,beta-unsaturated carbonyl compounds: from the Meyer-Schuster and Rupe rearrangements to redox isomerizations.
    Cadierno V; Crochet P; García-Garrido SE; Gimeno J
    Dalton Trans; 2010 May; 39(17):4015-31. PubMed ID: 20390164
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Iodo(III)-Meyer-Schuster Rearrangement of Propargylic Alcohols Promoted by Benziodoxole Triflate.
    Laskar RA; Ding W; Yoshikai N
    Org Lett; 2021 Feb; 23(3):1113-1117. PubMed ID: 33439023
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A simple and versatile re-catalyzed Meyer-Schuster rearrangement of propargylic alcohols to alpha,beta-unsaturated carbonyl compounds.
    Stefanoni M; Luparia M; Porta A; Zanoni G; Vidari G
    Chemistry; 2009; 15(16):3940-4. PubMed ID: 19283809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A general procedure for the synthesis of enones via gold-catalyzed Meyer-Schuster rearrangement of propargylic alcohols at room temperature.
    Pennell MN; Unthank MG; Turner P; Sheppard TD
    J Org Chem; 2011 Mar; 76(5):1479-82. PubMed ID: 21265538
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Catalytically Generated Vanadium Enolates Formed via Interruption of the Meyer-Schuster Rearrangement as Useful Reactive Intermediates.
    Trost BM; Tracy JS
    Acc Chem Res; 2020 Aug; 53(8):1568-1579. PubMed ID: 32692147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SOCl
    Jat RS; Bhanuchandra M
    J Org Chem; 2023 Sep; 88(18):13184-13190. PubMed ID: 37669462
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Meyer-Schuster rearrangement for the synthesis of alpha,beta-unsaturated carbonyl compounds.
    Engel DA; Dudley GB
    Org Biomol Chem; 2009 Oct; 7(20):4149-58. PubMed ID: 19795050
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis of α,β-Unsaturated Acylsilanes via Perrhenate-Catalyzed Meyer-Schuster Rearrangement of 1-Silylalkyn-3-ols.
    Nikolaev A; Orellana A
    Org Lett; 2015 Dec; 17(23):5796-9. PubMed ID: 26576952
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cu(II)-Catalyzed Decarboxylative (4 + 2) Annulation of Coumarin-3-Carboxylic Acids with In Situ Generated α,β-Unsaturated Carbonyl Compounds from
    Shankar M; Swamy KCK
    Org Lett; 2023 May; 25(19):3397-3401. PubMed ID: 37154427
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bi(OTf)
    Wang Z; Sun Y; Zhang Q; Pan W; Li T; Yin Y
    J Org Chem; 2022 Mar; 87(5):3329-3340. PubMed ID: 35147429
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Meyer-Schuster rearrangement of propargylic alcohols mediated by phosphorus-containing Brønsted acid catalysts.
    Radtanajiravong L; Peters J; Hummell J; Díez-González S
    Org Biomol Chem; 2022 Sep; 20(36):7338-7342. PubMed ID: 36073176
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cu/Fe-cocatalyzed Meyer-Schuster-like rearrangement of propargylic amines: direct access to E-β-aminoacryaldehydes.
    Chen M; Peng J; Mao T; Huang J
    Org Lett; 2014 Dec; 16(24):6286-9. PubMed ID: 25453833
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Competitive Gold-Promoted Meyer-Schuster and oxy-Cope Rearrangements of 3-Acyloxy-1,5-enynes: Selective Catalysis for the Synthesis of (+)-(S)-γ-Ionone and (-)-(2S,6 R)-cis-γ-Irone.
    Bugoni S; Merlini V; Porta A; Gaillard S; Zanoni G; Nolan SP; Vidari G
    Chemistry; 2015 Sep; 21(40):14068-74. PubMed ID: 26315968
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Meyer-Schuster-Type Rearrangement of Propargylic Alcohols into α-Selenoenals and -enones with Diselenides.
    Ban YL; You L; Feng KW; Ma FC; Jin XL; Liu Q
    J Org Chem; 2021 Apr; 86(7):5274-5283. PubMed ID: 33709711
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gold-Catalyzed Tandem Annulations of Pyridylhomopropargylic Alcohols with Propargyl Alcohols.
    Li XS; Xu DT; Niu ZJ; Li M; Shi WY; Wang CT; Wei WX; Liang YM
    Org Lett; 2021 Feb; 23(3):832-836. PubMed ID: 33507087
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intercepting the Gold-Catalysed Meyer-Schuster Rearrangement by Controlled Protodemetallation: A Regioselective Hydration of Propargylic Alcohols.
    Pennell MN; Kyle MP; Gibson SM; Male L; Turner PG; Grainger RS; Sheppard TD
    Adv Synth Catal; 2016 Apr; 358(9):1519-1525. PubMed ID: 29200990
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Formal Halo-Meyer-Schuster Rearrangement of Propargylic Acetates through a Novel Intermediate and an Unexampled Mechanistic Pathway.
    Sadhukhan S; Baire B
    Chemistry; 2019 Jul; 25(42):9816-9820. PubMed ID: 31141230
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Zn(OTf)
    Shan C; Chen F; Pan J; Gao Y; Xu P; Zhao Y
    J Org Chem; 2017 Nov; 82(21):11659-11666. PubMed ID: 29019674
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A coherent study on the Z-enoate assisted Meyer-Schuster rearrangement.
    Tharra P; Baire B
    Org Biomol Chem; 2017 Jul; 15(26):5579-5584. PubMed ID: 28639639
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.