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Volumn 51, Issue 25, 2006, Pages 5540-5547

An electrochemical alternative strategy to the synthesis of β-lactams. Part 2 [1]. C3{single bond}C4 bond formation

Author keywords

Lactams; Bromoamides; Cyclization; Organic electrosynthesis; Stereoselectivity

Indexed keywords

ELECTROLYSIS; ELECTROLYTES; SOLVENTS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 33746211264     PISSN: 00134686     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.electacta.2006.02.026     Document Type: Article
Times cited : (19)

References (41)
  • 3
    • 0004030275 scopus 로고
    • Page M.I. (Ed), Blackie Academic & Professional, New York
    • In: Page M.I. (Ed). The Chemistry of β-Lactams (1992), Blackie Academic & Professional, New York
    • (1992) The Chemistry of β-Lactams
  • 5
    • 0004030277 scopus 로고
    • Morin R.B., and Gorman M. (Eds), Academic Press, New York
    • In: Morin R.B., and Gorman M. (Eds). Chemistry and Biology of β-Lactam Antibiotics vols. 1-3 (1982), Academic Press, New York
    • (1982) Chemistry and Biology of β-Lactam Antibiotics , vol.1-3
  • 17
    • 0030028910 scopus 로고    scopus 로고
    • (and references therein)
    • Berks A.H. Tetrahedron 52 (1996) 331 (and references therein)
    • (1996) Tetrahedron , vol.52 , pp. 331
    • Berks, A.H.1
  • 38
    • 33746247480 scopus 로고    scopus 로고
    • K. Izutsu, Acid-Base Dissociation Constants in Dipolar Aprotic Solvents, IUPAC Chemical Data, Series No. 35, 1990.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.