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Volumn , Issue 3, 2009, Pages 338-341

An enantioselective synthesis of 3,4-benzo-5-oxacephams

Author keywords

Asymmetric synthesis; Chiral Lewis acids; Cyclization; Lactams

Indexed keywords


EID: 58649113013     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200800985     Document Type: Article
Times cited : (19)

References (38)
  • 7
    • 58649092677 scopus 로고    scopus 로고
    • W. Nagata, M. Narisada, T. Yoshida in Chemistry and Biology of β-Lactam Antibiotics (Ed.: R. B. M. Morin), Gorman, Academic Press, New York, 1982. p. 1 and references cited therein;
    • d) W. Nagata, M. Narisada, T. Yoshida in Chemistry and Biology of β-Lactam Antibiotics (Ed.: R. B. M. Morin), Gorman, Academic Press, New York, 1982. p. 1 and references cited therein;
  • 15
    • 0037631271 scopus 로고    scopus 로고
    • Z. Kałuża, R. Łysek, Tetrahedron: Asymmetry 1997, 8, 2553-2560;
    • e) Z. Kałuża, R. Łysek, Tetrahedron: Asymmetry 1997, 8, 2553-2560;
  • 29
    • 58649089415 scopus 로고    scopus 로고
    • 2] and various ligands (box-type, salen ligands) were tested. In all cases, the expected 3,4-benzo-5-oxacephams were formed in very low yields, as racemic mixtures.
    • 2] and various ligands (box-type, salen ligands) were tested. In all cases, the expected 3,4-benzo-5-oxacephams were formed in very low yields, as racemic mixtures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.