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Volumn 5, Issue 3, 2003, Pages 208-210

An efficient, stereoselective solid-phase synthesis of β-lactams using Mukaiyama's salt for the staudinger reaction

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; BETA LACTAM ANTIBIOTIC; KETENE DERIVATIVE; MONOBACTAM DERIVATIVE; SODIUM CHLORIDE;

EID: 0141786991     PISSN: 15204766     EISSN: None     Source Type: Journal    
DOI: 10.1021/cc020107d     Document Type: Article
Times cited : (65)

References (35)
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    • note
    • See Supporting Information for full details.
  • 29
    • 0141582195 scopus 로고    scopus 로고
    • note
    • 3N in anhydrous chloroform, and then 2-chloro-1-methylpyridinium iodide (4) was added. When the mixture became clear at 40°C, imine was added, and the reaction mixture was stirred at reflux for 2 h.
  • 31
    • 0141805370 scopus 로고    scopus 로고
    • note
    • During optimization, the major drawback was the formation of the amide 7 that can be formed by hydrolysis of the intermediates C or D (Scheme 2). Although strict anhydrous conditions are not required, the use of dry chloroform and rubber septa generally prevents this side reaction.


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