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Volumn 49, Issue 46, 2008, Pages 6508-6511

An efficient reduction protocol for the synthesis of β-hydroxycarbamates from β-nitro alcohols in one pot: a facile synthesis of (-)-β-conhydrine

Author keywords

Conhydrine; Hydroxy amine; Hydroxycarbamates; Nitro alcohols; Zn NH4Cl (aq)

Indexed keywords

AMINOALCOHOL; BETA HYDROXYCARBAMATE; CARBAMIC ACID DERIVATIVE; METHANOL; UNCLASSIFIED DRUG;

EID: 52949101693     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.08.113     Document Type: Article
Times cited : (29)

References (36)
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    • Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Springer, Berlin
    • In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis. 1st ed. (1999), Springer, Berlin
    • (1999) Comprehensive Asymmetric Catalysis. 1st ed.
  • 10
  • 25
    • 0004106186 scopus 로고    scopus 로고
    • McGraw-Hill, New York pp 258-263
    • Smith M.B. Oxidation. 2nd ed. Organic Synthesis (2002), McGraw-Hill, New York pp 258-263
    • (2002) Organic Synthesis
    • Smith, M.B.1
  • 34
    • 52949094294 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess (ee) was measured by HPLC analysis that was carried out using a Waters 510 HPLC system. A Chiracel OD packed in a SS column of 4.6 mm i.d. × 250 m was used. Isocratic elution was applied with a mobile phase consisting of n-hexane 90% and isopropanol 10% at a flow rate of 0.8 mL/min and a pressure of 125 psi. UV detection at 243 nm.
  • 35
    • 52949144975 scopus 로고    scopus 로고
    • For recent review on ring closing metathesis see:
    • For recent review on ring closing metathesis see:. Fürstner A. Angew. Chem., Int. Ed. 39 (2000) 3031-3043
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3031-3043
    • Fürstner, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.