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Volumn 3, Issue 5, 2001, Pages 727-729

One-pot direct conversion of 2,3-epoxy alcohols into enantiomerically pure 4-hydroxy-4,5-dihydroisoxazole 2-oxides

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALUMINUM DERIVATIVE; ALUMINUM LITHIUM HYDRIDE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; EPOXIDE; ISOXAZOLE DERIVATIVE; LITHIUM DERIVATIVE;

EID: 0035826324     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0070379     Document Type: Article
Times cited : (60)

References (24)
  • 1
    • 0000629986 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford
    • Padwa, A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 4, p 1069.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 1069
    • Padwa, A.1
  • 15
    • 0025266963 scopus 로고
    • (a) Rosini, G.; Galarini, R.; Marotta, E.; Righi, P. J. Org. Chem. 1990, 55, 781. For a review on the nitroaldol reaction, see: Rosini, G. The Henry (Nitroaldol) Reaction. In Comprehensive Organic Synthesis; Trost, B. M., Heathcock, C. H., Eds; Pergamon Press: Oxford, 1991; Vol. 2, p 321.
    • (1990) J. Org. Chem. , vol.55 , pp. 781
    • Rosini, G.1    Galarini, R.2    Marotta, E.3    Righi, P.4
  • 16
    • 0000851805 scopus 로고
    • The Henry (Nitroaldol) reaction
    • Trost, B. M., Heathcock, C. H., Eds; Pergamon Press: Oxford
    • (a) Rosini, G.; Galarini, R.; Marotta, E.; Righi, P. J. Org. Chem. 1990, 55, 781. For a review on the nitroaldol reaction, see: Rosini, G. The Henry (Nitroaldol) Reaction. In Comprehensive Organic Synthesis; Trost, B. M., Heathcock, C. H., Eds; Pergamon Press: Oxford, 1991; Vol. 2, p 321.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 321
    • Rosini, G.1
  • 20
    • 7044235263 scopus 로고    scopus 로고
    • For a clear explanation of the terms tandem, consecutive, and domino process, see: Tietze, L. Chem. Rev. 1996, 96, 115.
    • (1996) Chem. Rev. , vol.96 , pp. 115
    • Tietze, L.1
  • 23
    • 0042908324 scopus 로고    scopus 로고
    • note
    • See Supporting Information for full details.
  • 24
    • 0041906280 scopus 로고    scopus 로고
    • note
    • 4 ring cleavage, a reduction-elimination of the ester function with concomitant ring opening afforded the corresponding 3-hydroxy nitrile in moderate yields.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.