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Volumn 63, Issue 46, 2007, Pages 11421-11428

A general and enantiodivergent method for the asymmetric synthesis of piperidine alkaloids: concise synthesis of (R)-pipecoline, (S)-coniine and other 2-alkylpiperidines

Author keywords

[No Author keywords available]

Indexed keywords

AMINOALCOHOL; CONIINE; PIPECOLINE; PIPERIDINE DERIVATIVE; PSEUDOEPHEDRINE; UNCLASSIFIED DRUG;

EID: 34848902601     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.08.067     Document Type: Article
Times cited : (13)

References (45)
  • 1
    • 34848884051 scopus 로고    scopus 로고
    • For some reviews see:
  • 16
    • 34848875538 scopus 로고    scopus 로고
    • For other selected synthetic approaches to enantioenriched alkylpiperidines from β-amino carbonyl derivatives, see:
  • 30
    • 34848841948 scopus 로고    scopus 로고
    • note
    • In some cases (S)-configurated derivatives were obtained as a result of the application of CIP rules.
  • 31
    • 34848870987 scopus 로고    scopus 로고
    • For some selected examples on the formation of piperidines via intramolecular reductive amination see:
  • 43
    • 0042865048 scopus 로고    scopus 로고
    • 20 +3.9 (c 1.1, EtOH) for a sample of (R)-pipecoline hydrochloride obtained by us; lit. +3.97 (c 1.0, EtOH).
    • 20 +3.9 (c 1.1, EtOH) for a sample of (R)-pipecoline hydrochloride obtained by us; lit. +3.97 (c 1.0, EtOH). Andres J.M., Herraiz-Sierra I., Pedrosa R., and Perez-Encabo A. Eur. J. Org. Chem. (2000) 1719
    • (2000) Eur. J. Org. Chem. , pp. 1719
    • Andres, J.M.1    Herraiz-Sierra, I.2    Pedrosa, R.3    Perez-Encabo, A.4
  • 45
    • 34848924716 scopus 로고    scopus 로고
    • note
    • 20 +9.4 (c 0.2, EtOH). See Refs. 7 and 8.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.