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Journal Abstract Search

188 related items for PubMed ID: 15727479

  • 1. Asymmetric synthesis of (+)-(S,S)-reboxetine via a new (S)-2-(hydroxymethyl)morpholine preparation.
    Brenner E, Baldwin RM, Tamagnan G.
    Org Lett; 2005 Mar 03; 7(5):937-9. PubMed ID: 15727479
    [Abstract] [Full Text] [Related]

  • 2. Concise synthesis of (S)-N-BOC-2-hydroxymethylmorpholine and (S)-N-BOC-morpholine-2-carboxylic acid.
    Henegar KE.
    J Org Chem; 2008 May 02; 73(9):3662-5. PubMed ID: 18363360
    [Abstract] [Full Text] [Related]

  • 3. Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of beta-amino alcohols.
    Métro TX, Pardo DG, Cossy J.
    J Org Chem; 2008 Jan 18; 73(2):707-10. PubMed ID: 18092801
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  • 7. Efficient synthesis of NK(1) receptor antagonist aprepitant using a crystallization-induced diastereoselective transformation.
    Brands KM, Payack JF, Rosen JD, Nelson TD, Candelario A, Huffman MA, Zhao MM, Li J, Craig B, Song ZJ, Tschaen DM, Hansen K, Devine PN, Pye PJ, Rossen K, Dormer PG, Reamer RA, Welch CJ, Mathre DJ, Tsou NN, McNamara JM, Reider PJ.
    J Am Chem Soc; 2003 Feb 26; 125(8):2129-35. PubMed ID: 12590540
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  • 9. Stereoselective synthesis of (2S,3R)- and (2R,3S)-iodoreboxetine; potential SPECT imaging agents for the noradrenaline transporter.
    Jobson NK, Spike R, Crawford AR, Dewar D, Pimlott SL, Sutherland A.
    Org Biomol Chem; 2008 Jul 07; 6(13):2369-76. PubMed ID: 18563271
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  • 10. Stereoselective cyclopropanation of serine- and threonine-derived oxazines to access new morpholine-based scaffolds.
    Sladojevich F, Trabocchi A, Guarna A.
    Org Biomol Chem; 2008 Sep 21; 6(18):3328-36. PubMed ID: 18802639
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  • 11. First total synthesis of antimitotic compound, (+)-phomopsidin.
    Suzuki T, Usui K, Miyake Y, Namikoshi M, Nakada M.
    Org Lett; 2004 Feb 19; 6(4):553-6. PubMed ID: 14961621
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  • 12. Efficient, stereoselective synthesis of trans-2,5-disubstituted morpholines.
    Lanman BA, Myers AG.
    Org Lett; 2004 Mar 18; 6(6):1045-7. PubMed ID: 15012096
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  • 13. Design and synthesis of reboxetine analogs morpholine derivatives as selective norepinephrine reuptake inhibitors.
    Xu W, Gray DL, Glase SA, Barta NS.
    Bioorg Med Chem Lett; 2008 Oct 15; 18(20):5550-3. PubMed ID: 18805691
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  • 14. Preparation of new chiral building blocks: highly enantioselective reduction of prochiral 1,3-cycloalkanediones possessing a methyl group and a protected hydroxymethyl group at their C2 position with baker's yeast or CBS catalyst.
    Watanabe H, Iwamoto M, Nakada M.
    J Org Chem; 2005 Jun 10; 70(12):4652-8. PubMed ID: 15932301
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  • 15. Direct access to marine pyrrole-2-aminoimidazoles, oroidin, and derivatives, via new acyl-1,2-dihydropyridin intermediates.
    Schroif-Gregoire C, Travert N, Zaparucha A, Al-Mourabit A.
    Org Lett; 2006 Jul 06; 8(14):2961-4. PubMed ID: 16805527
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  • 16. Crystallization-induced chiral inversion as the key step for synthesis of (S)-2-acetylthio-3-phenylpropanoic acid from l-phenylalanine.
    Chen JG, Zhu J, Skonezny PM, Rosso V, Venit JJ.
    Org Lett; 2004 Sep 16; 6(19):3233-5. PubMed ID: 15355020
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  • 17. A new entry to Pd-H chemistry: catalytic asymmetric conjugate reduction of enones with EtOH and a highly enantioselective synthesis of warfarin.
    Tsuchiya Y, Hamashima Y, Sodeoka M.
    Org Lett; 2006 Oct 12; 8(21):4851-4. PubMed ID: 17020319
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  • 18. Enantioselective synthesis of alpha-ionone derivatives using an anti S(N)2' substitution of functionalized zinc organometallics.
    Soorukram D, Knochel P.
    Org Lett; 2004 Jul 08; 6(14):2409-11. PubMed ID: 15228291
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  • 19. Total synthesis of (+)-boronolide, (+)-deacetylboronolide, and (+)-dideacetylboronolide.
    Chandrasekhar M, Chandra KL, Singh VK.
    J Org Chem; 2003 May 16; 68(10):4039-45. PubMed ID: 12737588
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  • 20. Direct asymmetric catalytic thienylaluminum addition to ketones: a concise approach to the synthesis of (S)-tiemonium iodide.
    Biradar DB, Zhou S, Gau HM.
    Org Lett; 2009 Aug 06; 11(15):3386-9. PubMed ID: 19588914
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