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Volumn 14, Issue 2-3, 2002, Pages 169-172

Enantioselective carbon-hydrogen insertion is an effective and efficient methodology for the synthesis of (R)-(-)-baclofen

Author keywords

Catalytic enantioselective synthesis; Chiral dirhodium(II) carboxamidates; Diazoacetate; Metal carbene reactions

Indexed keywords

4 AMINOBUTYRIC ACID RECEPTOR STIMULATING AGENT; BACLOFEN;

EID: 0036151961     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.10060     Document Type: Article
Times cited : (39)

References (16)
  • 4
    • 0034727937 scopus 로고    scopus 로고
    • Enantioselective Michael addition of nitromethane to α,β-enones catalyzed by chiral quaternary ammonium salts. A simple synthesis of (R)-baclofen
    • (2000) Organic Lett , vol.2 , pp. 4257-4259
    • Corey, E.J.1    Zhang, F.-Y.2
  • 16
    • 0031983769 scopus 로고    scopus 로고
    • Enantioselective synthesis of 4-substituted 2-pyrrolidinones by site-selective C-H insertion of α-methoxycarbonyl-α-diazoacetanilides catalyzed by dirhodium(II) tetrakis [N-phtaloyl-(S)-tert-leucinate]
    • (1998) Tetrahedron Lett , vol.39 , pp. 79-82
    • Anada, M.1    Hashimoto, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.