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Volumn 6, Issue , 2002, Pages 270-311

Chiral β-aminoalcohols and derivatives in the asymmetric synthesis of tetrahydroisoquinolines

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EID: 77954700187     PISSN: 17249449     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Article
Times cited : (4)

References (266)
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  • 3
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    • Bentley, K.W.1
  • 7
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    • For a review on Stevens rearrangements see, Trost, B. M.; Fleming, I.; Pattenden I., Eds.; Pergamon: Oxford
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    • Markó, I.E.1
  • 42
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    • This derivative was prepared from (S)-DOPA, according to a patent, U.S. Patent 4,344,949
    • This derivative was prepared from (S)-DOPA, according to a patent: Hoefle, M. L.; Klutchko, S. to Warner-Lambert Company. U.S. Patent 4,344,949, 1982.
    • (1982) Warner-Lambert Company
    • Hoefle, M.L.1    Klutchko, S.2
  • 135
    • 33847086285 scopus 로고
    • When the 1H-NMR spectra were carried out in CDCl3, equilibrium mixtures of the imines 2 and the corresponding tautomeric oxazolidines were observed, whereas the 1H-NMR in CD3OD showed resonances for only the open chain structures. For studies in imine-oxazolidine tautomerism see:
    • When the 1H-NMR spectra were carried out in CDCl3, equilibrium mixtures of the imines 2 and the corresponding tautomeric oxazolidines were observed, whereas the 1H-NMR in CD3OD showed resonances for only the open chain structures. For studies in imine-oxazolidine tautomerism see: (a). Lambert, J. B.; Majchrzak, M. W. J. Am. Chem. Soc. 1980, 102, 3588.
    • (1980) J. Am. Chem. Soc , vol.102 , pp. 3588
    • Lambert, J.B.1    Majchrzak, M.W.2
  • 150
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    • For syntheses of natural and non natural isopavines see, for example, Academic Press: New York
    • For syntheses of natural and non natural isopavines see, for example: Gözler, B. In The Alkaloids; Academic Press: New York, 1987; vol. 31, pp. 342.
    • (1987) The Alkaloids , vol.31 , pp. 342
    • Gözler, B.1
  • 156
    • 0002934578 scopus 로고
    • See also refs. Errore. Il segnalibro non è definito. and 80
    • Rice, K. C.; Ripka, W. C.; Reden, J.; Brossi, A. J. Org. Chem. 1980, 45, 601. See also refs. Errore. Il segnalibro non è definito. and 80.
    • (1980) J. Org. Chem. , vol.45 , pp. 601
    • Rice, K.C.1    Ripka, W.C.2    Reden, J.3    Brossi, A.4
  • 214
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    • For a review on electrophilic amination reagents see
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    • (1997) Synlett , pp. 741
    • Greck, C.1    Genêt, J.P.2
  • 226
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    • Ed.: Ahmed F. Abdel-Magid. ACS Symposium Series 641. Washington
    • Gribble, G. W. Reductions in Organic Synthesis, Ed.: Ahmed F. Abdel-Magid. ACS Symposium Series 641. Washington 1996, pp. 167-200.
    • (1996) Reductions in Organic Synthesis , pp. 167-200
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  • 244
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    • Arylacetic acids were converted by oxidation of the aryl ring into N-Boc -aminoacids
    • Arylacetic acids were converted by oxidation of the aryl ring into N-Boc -aminoacids: Fodor, G.; Csepreghy, G. J. Chem. Soc. 1961, 3222.
    • (1961) J. Chem. Soc. , pp. 3222
    • Fodor, G.1    Csepreghy, G.2


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