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Volumn , Issue 9, 1999, Pages 855-856

A simple entry towards novel bi- and tricyclic N-oxy-β-lactams by high pressure promoted tandem [4+2]/[3+2] cycloadditions of enol ethers and β-nitrostyrene

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAM ANTIBIOTIC; ETHER DERIVATIVE; STYRENE DERIVATIVE;

EID: 0033532232     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a901505a     Document Type: Article
Times cited : (33)

References (17)
  • 4
    • 20444470003 scopus 로고
    • Chem. Abstr., 1986, 105, 60477.
    • (1986) Chem. Abstr. , vol.105 , pp. 60477
  • 5
    • 0030062476 scopus 로고    scopus 로고
    • and refs. cited therein
    • Overview of multicyclic β-lactams (not heteroatom activated); C. Niu, T. Pettersson and M. J. Miller, J. Org. Chem., 1996, 61, 1014 and refs. cited therein.
    • (1996) J. Org. Chem. , vol.61 , pp. 1014
    • Niu, C.1    Pettersson, T.2    Miller, M.J.3
  • 11
    • 85087252043 scopus 로고    scopus 로고
    • note
    • 2-hexane. X-Ray analysis confirmed the configuration assigned by 2D-NOESY analysis. Product 5b is formed via a base-promoted epimerisation of 5a.
  • 17
    • 20444485119 scopus 로고    scopus 로고
    • Further investigations concerning the regioselectivity of the [3+2] cycloadditions are in progress
    • Further investigations concerning the regioselectivity of the [3+2] cycloadditions are in progress.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.