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Volumn , Issue 11, 2008, Pages 1901-1909

Diastereoselective additions to (3S)-3-aminodehydrocaprolactams: Development of a versatile synthesis of new substituted cyclic L-lysines

Author keywords

3 aminocaprolactam; Anchimeric assistance; Azidomethoxylation; Diastereoselective addition; Halomethoxylation

Indexed keywords


EID: 53749104917     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200701004     Document Type: Article
Times cited : (10)

References (43)
  • 8
    • 53749088824 scopus 로고    scopus 로고
    • D. J. Grainger, D. J. Fox, PCT Int. WO 2006016152 A1 20060216, CAN 144:232931;
    • d) D. J. Grainger, D. J. Fox, PCT Int. WO 2006016152 A1 20060216, CAN 144:232931;
  • 32
    • 53749101876 scopus 로고    scopus 로고
    • 4 interacts in a concerted manner with C-6 and C-7, which leads to a bicyclic osmate.
    • 4 interacts in a concerted manner with C-6 and C-7, which leads to a bicyclic osmate.
  • 38
    • 53749087356 scopus 로고    scopus 로고
    • The mesylate of 6-hydroxy-7-methoxycaprolactam 4 was also unreactive towards cyanide nucleophiles at room temperature.
    • The mesylate of 6-hydroxy-7-methoxycaprolactam 4 was also unreactive towards cyanide nucleophiles at room temperature.
  • 41
    • 53749098269 scopus 로고    scopus 로고
    • 3J = 3.5 Hz instead of triplet or dd, as one may expect for this proton in 13′) were unambiguously consistent with the relative configuration of compound 13.
    • 3J = 3.5 Hz instead of triplet or dd, as one may expect for this proton in 13′) were unambiguously consistent with the relative configuration of compound 13.
  • 42
    • 53749106238 scopus 로고    scopus 로고
    • See supplementary material for NMR spectroscopic data of compound 13.
    • See supplementary material for NMR spectroscopic data of compound 13.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.