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Volumn 63, Issue 20, 2007, Pages 4278-4283

A new enantiodivergent synthesis of the Geissman-Waiss lactone

Author keywords

1,2 Oxazinanes; Aminooxy compounds; Asymmetric synthesis; Michael addition

Indexed keywords

2 OXA 6 AZABICYCLO[3.3.0]OCTAN 3 ONE; ESTER DERIVATIVE; LACTONE DERIVATIVE; METHYL 6 (TERT BUTOXYCARBONYLAMINO)OXY 4 HYDROXY 2 HEXENOATE; NITROGEN; OXYGEN; TERT BUTYL 3 HYDROXY 4 PENTENOATE; UNCLASSIFIED DRUG;

EID: 34047264016     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.03.056     Document Type: Article
Times cited : (11)

References (39)
  • 30
    • 34047259470 scopus 로고    scopus 로고
    • note
    • The crude aldehyde obtained upon work-up was sufficiently pure to be used in the next step without further purification, analytical and spectroscopic data matching those reported in Ref. 20.
  • 33
    • 33744501288 scopus 로고    scopus 로고
    • For preparation of O-substituted hydroxylamines from alcohols, see also:
    • For preparation of O-substituted hydroxylamines from alcohols, see also:. Albrecht S., Defoin A., and Tarnus C. Synthesis (2006) 1635
    • (2006) Synthesis , pp. 1635
    • Albrecht, S.1    Defoin, A.2    Tarnus, C.3
  • 34
    • 34047258818 scopus 로고    scopus 로고
    • note
    • 1H NMR spectrum of the crude reaction mixture.
  • 36
    • 34047267442 scopus 로고    scopus 로고
    • For a recent application of aminooxy derivatives in a conjugate addition/intramolecular Wittig reaction sequence allowing for the synthesis of chiral dihydro-[1,2]-oxazines, see:
  • 39
    • 34047265115 scopus 로고    scopus 로고
    • note
    • 3) being given for the (S)-configured alcohol.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.