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Volumn , Issue 6, 2004, Pages 1029-1033

Electrooxidation based strategy towards the core 3-amino-6-hydroxy-azepan- 2-one

Author keywords

Bengamides; Diastereoselectivity; Dihydroxylation; Electrooxidation; Osmium

Indexed keywords

LYSINE DERIVATIVE;

EID: 3142752550     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-820048     Document Type: Article
Times cited : (7)

References (48)
  • 22
    • 0000435096 scopus 로고
    • (a) Shono, T. Tetrahedron 1984, 40, 811-850.
    • (1984) Tetrahedron , vol.40 , pp. 811-850
    • Shono, T.1
  • 33
    • 3142707411 scopus 로고    scopus 로고
    • note
    • 4 as electrolytes were less successful.
  • 37
    • 3142776464 scopus 로고    scopus 로고
    • note
    • We observed similar C=C reductions when endocyclic enecarbamates derived from pipecolic acid were submitted to hydroboration with borane or dihaloboranes (unpublished results).
  • 42
    • 3142679572 scopus 로고    scopus 로고
    • note
    • The osmylation/acetylation sequence carried out with substrate 5c gave a mixture of the expected diacetate 7c contamined by a bicyclic aminal resulting from intramolecular displacement of the hemiaminal hydroxy group via the corresponding iminium ion.
  • 48
    • 3142656007 scopus 로고    scopus 로고
    • note
    • Indeed, examination of the IR spectra showed no significant changes in the lactam carbonyl absorption between lactams 4 or 3 and enamides 2 or 5.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.