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Volumn 61, Issue 15, 2005, Pages 3725-3731

Stereoselective synthesis of (3S,4S)-tert-butyl-N-Boc-3-ethyl-4-hydroxy-l- prolinate and (3S,4R)-tert-butyl-N-Boc-3-ethyl-4-hydroxy-l-prolinate

Author keywords

4 Hydroxyproline derivatives; Asymmetric reduction; Luche reagent

Indexed keywords

PROLINE DERIVATIVE; TERT BUTYL N TERT BUTYLOXYCARBONYL 3 ETHYL 4 HYDROXYLPROLINATE; UNCLASSIFIED DRUG;

EID: 15044355375     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.02.006     Document Type: Article
Times cited : (12)

References (35)
  • 7
    • 0037164661 scopus 로고    scopus 로고
    • For current examples and leading references to the synthesis of substituted prolines using nucleophilic displacement or addition reactions, see: (b) C. Flamant-Robin, Q. Wang, A. Chiaroni, and N.A. Sasaki Tetrahedron 58 2002 10475 10484
    • (2002) Tetrahedron , vol.58 , pp. 10475-10484
    • Flamant-Robin, C.1    Wang, Q.2    Chiaroni, A.3    Sasaki, N.A.4
  • 16
    • 0037459690 scopus 로고    scopus 로고
    • For current examples and leading references to the synthesis of substituted prolines using amino-zinc-enolate carbometalation reactions, see: (k) P. Karoyan, J. Quancard, J. Vaissermann, and G. Chassaing J. Org. Chem. 68 2003 2256 2265
    • (2003) J. Org. Chem. , vol.68 , pp. 2256-2265
    • Karoyan, P.1    Quancard, J.2    Vaissermann, J.3    Chassaing, G.4
  • 28
    • 85030810585 scopus 로고    scopus 로고
    • www.3dgenoscience.com
  • 35
    • 85030814523 scopus 로고    scopus 로고
    • note
    • Since compound 2 was always obtained as an oil, X-ray studies were impossible to undertake.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.