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Volumn , Issue 15, 2007, Pages 2321-2330

Synthesis of β-lactams using the Kinugasa reaction

Author keywords

Lactams; Alkynes; Cycloadditions; Kinugasa reaction; Nitrones

Indexed keywords

ALKYNE; AZETIDINE; BETA LACTAM; CUPROUS ION; NITRONE; OXAZIRIDINE DERIVATIVE; PROLINE;

EID: 34948844484     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-986637     Document Type: Review
Times cited : (44)

References (57)
  • 4
    • 0025991820 scopus 로고
    • (a) Chain, B. Nature 1991, 353, 492.
    • (1991) Nature , vol.353 , pp. 492
    • Chain, B.1
  • 18
    • 33646544385 scopus 로고    scopus 로고
    • It is generally accepted that the Staudinger reaction proceeds stepwise via a zwitterionic intermediate and not via a concerted pericyclic reaction: (b) Jiao, L.; Liang, Y.; Xu, J. J. Am. Chem. Soc. 2006, 128, 6060.
    • It is generally accepted that the Staudinger reaction proceeds stepwise via a zwitterionic intermediate and not via a concerted pericyclic reaction: (b) Jiao, L.; Liang, Y.; Xu, J. J. Am. Chem. Soc. 2006, 128, 6060.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.