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Volumn 50, Issue 17, 2009, Pages 1943-1946

Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (-)-Paroxetine

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; PAROXETINE; PIPERIDINE DERIVATIVE;

EID: 61749096057     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.02.049     Document Type: Article
Times cited : (92)

References (48)
  • 1
    • 7044235263 scopus 로고    scopus 로고
    • For two excellent summaries on the concept of domino and tandem reactions see:
    • For two excellent summaries on the concept of domino and tandem reactions see:. Tietze L.F. Chem. Rev., 96 (1996) 115-136
    • (1996) Chem. Rev. , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 3
    • 33646573235 scopus 로고    scopus 로고
    • For selected examples in the literature:
    • For selected examples in the literature:. Ibrahem I., and Córdova A. Angew. Chem., Int. Ed. 45 (2006) 1952-1956
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 1952-1956
    • Ibrahem, I.1    Córdova, A.2
  • 19
    • 61749086252 scopus 로고
    • Pelletier S.W. (Ed), John Wiley & Sons, New York
    • Elbein D.A., and Molineux R. In: Pelletier S.W. (Ed). Alkaloids; Chemical and Biological Prospective. Vol. 57 (1987), John Wiley & Sons, New York
    • (1987) Vol. 57
    • Elbein, D.A.1    Molineux, R.2
  • 35
    • 34250613134 scopus 로고    scopus 로고
    • For recent reviews of asymmetric organocatalytic 1,4-conjugated additions, see:
    • For recent reviews of asymmetric organocatalytic 1,4-conjugated additions, see:. Tsogoeva S.B. Eur. J. Org. Chem. (2007) 1701-1716
    • (2007) Eur. J. Org. Chem. , pp. 1701-1716
    • Tsogoeva, S.B.1
  • 38
    • 61749102346 scopus 로고    scopus 로고
    • Rubidium and potassium salts of proline has been used in the synthesis of piperidines. De Ferra, L.; Massardo, P.; Piccolo, O.; Cignarella G. U.S. 6,444,822, B1.
    • Rubidium and potassium salts of proline has been used in the synthesis of piperidines. De Ferra, L.; Massardo, P.; Piccolo, O.; Cignarella G. U.S. 6,444,822, B1.
  • 41
    • 61749089595 scopus 로고    scopus 로고
    • note
    • ® IA hexane/IPA 90:10 1 mL/min. Time: 19.3 min and 35.4 min.
  • 47
    • 58249101213 scopus 로고    scopus 로고
    • note
    • During preparation of this Letter, Dr. J. Franzén reported an excellent synthesis of quinolizilidine derivatives based on this concept: Franzén, J.; Fisher, A. Angew. Chem., Int. Ed. 2009. doi:10.1002/anie.200805130.
  • 48
    • 61749093558 scopus 로고    scopus 로고
    • note
    • Crystallographic data for structural analysis have been deposited with the Cambridge Crystallographic Data Centre, CCDC No. 719613.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.