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Journal Abstract Search

165 related items for PubMed ID: 23677770

  • 1. Synthesis of 1-substituted tetrahydroisoquinolines by lithiation and electrophilic quenching guided by in situ IR and NMR spectroscopy and application to the synthesis of salsolidine, carnegine and laudanosine.
    Li X, Leonori D, Sheikh NS, Coldham I.
    Chemistry; 2013 Jun 10; 19(24):7724-30. PubMed ID: 23677770
    [Abstract] [Full Text] [Related]

  • 2. Synthesis of substituted tetrahydroisoquinolines by lithiation then electrophilic quench.
    Talk RA, Duperray A, Li X, Coldham I.
    Org Biomol Chem; 2016 Jun 07; 14(21):4908-17. PubMed ID: 27169500
    [Abstract] [Full Text] [Related]

  • 3. Synthesis of 1,1-disubstituted tetrahydroisoquinolines by lithiation and substitution, with in situ IR spectroscopy and configurational stability studies.
    Li X, Coldham I.
    J Am Chem Soc; 2014 Apr 16; 136(15):5551-4. PubMed ID: 24707968
    [Abstract] [Full Text] [Related]

  • 4. Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench.
    Carter N, Li X, Reavey L, Meijer AJHM, Coldham I.
    Chem Sci; 2018 Feb 07; 9(5):1352-1357. PubMed ID: 29675183
    [Abstract] [Full Text] [Related]

  • 5. Synthesis of Tetrahydroisoquinoline Alkaloids and Related Compounds through the Alkylation of Anodically Prepared α-Amino Nitriles.
    Benmekhbi L, Louafi F, Roisnel T, Hurvois JP.
    J Org Chem; 2016 Aug 05; 81(15):6721-39. PubMed ID: 27410716
    [Abstract] [Full Text] [Related]

  • 6. Tetrahydroisoquinoline and beta-carboline alkaloids from Haloxylon articulatum (Cav.) Bunge (Chenopodiaceae).
    El-Shazly A, Wink M.
    Z Naturforsch C J Biosci; 2003 Aug 05; 58(7-8):477-80. PubMed ID: 12939030
    [Abstract] [Full Text] [Related]

  • 7. Synthesis of tetrahydroisoquinoline alkaloids via anodic cyanation as the key step.
    Louafi F, Hurvois JP, Chibani A, Roisnel T.
    J Org Chem; 2010 Aug 20; 75(16):5721-4. PubMed ID: 20704442
    [Abstract] [Full Text] [Related]

  • 8. An experimental and in situ IR spectroscopic study of the lithiation-substitution of N-Boc-2-phenylpyrrolidine and -piperidine: controlling the formation of quaternary stereocenters.
    Sheikh NS, Leonori D, Barker G, Firth JD, Campos KR, Meijer AJ, O'Brien P, Coldham I.
    J Am Chem Soc; 2012 Mar 21; 134(11):5300-8. PubMed ID: 22339321
    [Abstract] [Full Text] [Related]

  • 9. Asymmetric Synthesis of 2-Arylindolines and 2,2-Disubstituted Indolines by Kinetic Resolution.
    Choi A, El-Tunsi A, Wang Y, Meijer AJHM, Li J, Li X, Proietti Silvestri I, Coldham I.
    Chemistry; 2021 Aug 11; 27(45):11670-11675. PubMed ID: 34110662
    [Abstract] [Full Text] [Related]

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  • 11. Enantioselective synthesis of 2-substituted 2-phenylethylamines by lithiation-substitution sequences: synthetic development and mechanistic pathway.
    Laumer JM, Kim DD, Beak P.
    J Org Chem; 2002 Sep 20; 67(19):6797-804. PubMed ID: 12227812
    [Abstract] [Full Text] [Related]

  • 12. New strategy for the synthesis of tetrahydroisoquinoline alkaloids.
    Magnus P, Matthews KS, Lynch V.
    Org Lett; 2003 Jun 12; 5(12):2181-4. PubMed ID: 12790559
    [Abstract] [Full Text] [Related]

  • 13. [Competitive inhibition of catechol-O-methyltransferase by the tetrahydroisoquinoline alkaloids salsolidine and 1-carboxysalsoline].
    Sanft K, Thomas H.
    Z Naturforsch C J Biosci; 1989 Jun 12; 44(1-2):173-6. PubMed ID: 2490067
    [Abstract] [Full Text] [Related]

  • 14. Preparation of 1-Substituted Tetrahydro-β-carbolines by Lithiation-Substitution.
    Cochrane EJ, Hassall LA, Coldham I.
    J Org Chem; 2015 Jun 05; 80(11):5964-9. PubMed ID: 25974712
    [Abstract] [Full Text] [Related]

  • 15. Stereospecific N-methylation of the tetrahydroisoquinoline alkaloids isosalsoline and salsolidine by amine N-methyltransferase A from bovine liver.
    Bahnmaier AH, Woesle B, Thomas H.
    Chirality; 1999 Jun 05; 11(2):160-5. PubMed ID: 9951405
    [Abstract] [Full Text] [Related]

  • 16. Asymmetric Total Syntheses of (-)-Fennebricin A, (-)-Renieramycin J, (-)-Renieramycin G, (-)-Renieramycin M, and (-)- Jorunnamycin A via C-H Activation.
    Zheng Y, Li XD, Sheng PZ, Yang HD, Wei K, Yang YR.
    Org Lett; 2020 Jun 05; 22(11):4489-4493. PubMed ID: 32437173
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  • 18. [Asymmetric reactions based on activation and structure control of molecule--asymmetric reaction of lithiated nucleophiles].
    Tomioka K.
    Yakugaku Zasshi; 2004 Feb 05; 124(2):43-53. PubMed ID: 14978947
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