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Volumn , Issue 7, 2006, Pages 1113-1115

Enantioselective synthesis of β-lactams using a chiral auxiliary

Author keywords

lactams; Enantioselectivity; Imines; Reformatsky reaction

Indexed keywords

3 ETHYL 1 PHENYL 4 STYRYLAZETIDIN 2 ONE; 4 (4 CHLOROPHENYL) 3 METHYL 1 PHENYLAZETIDIN 2 ONE; BETA LACTAM DERIVATIVE; IMINE; UNCLASSIFIED DRUG;

EID: 33646672613     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-939082     Document Type: Article
Times cited : (14)

References (24)
  • 7
    • 0004030277 scopus 로고
    • Morin, R. B.; Gorman, M., Eds.; Academic Press: New York
    • (d) Chemistry and Biology of β-Lactam Antibiotics, Vol. 1-3; Morin, R. B.; Gorman, M., Eds.; Academic Press: New York, 1982.
    • (1982) Chemistry and Biology of β-Lactam Antibiotics , vol.1-3
  • 10
    • 0004030275 scopus 로고
    • Page, M. J., Ed.; Chapman and Hall: London
    • (g) The Chemistry of β-Lactams; Page, M. J., Ed.; Chapman and Hall: London, 1992.
    • (1992) The Chemistry of β-Lactams
  • 22
    • 33646712230 scopus 로고    scopus 로고
    • note
    • +.
  • 24
    • 33646701294 scopus 로고    scopus 로고
    • Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK; fax: +44(1223)336033; or deposit@ccdc.cam.ac.uk
    • CCDC 273640 contains the supplementary crystallographic data (excluding structure factors) for compound 3b. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html [or from the Cambridge Crystallographic Data Centre, 12, Union Road, Cambridge CB2 1EZ, UK; fax: +44(1223)336033; or deposit@ccdc.cam.ac.uk].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.