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Volumn , Issue 14, 2005, Pages 2335-2340

Stereoselective entry to bicyclic β-lactams via free radical cyclization of 2-azetidinone-tethered bromohomoallylic alcohols

Author keywords

Carbonyl additions; Cyclizations; Lactams; Radical reactions; Tin

Indexed keywords

MOLECULAR STRUCTURE; REACTION KINETICS; SOLUTIONS; SYNTHESIS (CHEMICAL); TIN;

EID: 24944519743     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-869985     Document Type: Article
Times cited : (8)

References (42)
  • 1
    • 3042624178 scopus 로고    scopus 로고
    • (a) Hot Topic: β-Lactams: Synthesis, Stereochemistry, Synthons, and Biological Evaluation: Banik, B. K. Curr. Med. Chem. 2004, 11, issue 14.
    • (2004) Curr. Med. Chem. , vol.11 , Issue.14
    • Banik, B.K.1
  • 34
    • 0033804280 scopus 로고    scopus 로고
    • The synthesis of medium-sized rings has usually been hampered by entropic/enthalpic factors and transannular interactions between the methylene groups. For reviews see: (a) Galli, L.; Mandolini, L. Eur. J. Org. Chem. 2000, 3117.
    • (2000) Eur. J. Org. Chem. , pp. 3117
    • Galli, L.1    Mandolini, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.