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Volumn 49, Issue 19, 2008, Pages 3078-3082

Synthetic utility of epoxides for chiral functionalization of isoxazoles

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; BENZYLIC EPOXIDE DERIVATIVE; EPOXIDE; ISOXAZOLE DERIVATIVE; PROPYLENE OXIDE; STYRENE OXIDE; UNCLASSIFIED DRUG; VINYLIC EPOXIDE DERIVATIVE;

EID: 41649100264     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.03.059     Document Type: Article
Times cited : (3)

References (44)
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    • Jacobsen E.N., and Wu M.H. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis II Vol. 2 (1999), Springer, Berlin 621-677
    • (1999) Comprehensive Asymmetric Catalysis II , vol.2 , pp. 621-677
    • Jacobsen, E.N.1    Wu, M.H.2
  • 10
    • 41649113150 scopus 로고    scopus 로고
    • Smith, M. P., Ph.D. Dissertation, University of Idaho, 1993.
    • Smith, M. P., Ph.D. Dissertation, University of Idaho, 1993.
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    • 41649116665 scopus 로고    scopus 로고
    • Burns, C. T.; Natale, N. R. In 49th Northwest Regional ACS Meeting, Anchorage Alaska, June 15-18, 1994.
    • Burns, C. T.; Natale, N. R. In 49th Northwest Regional ACS Meeting, Anchorage Alaska, June 15-18, 1994.
  • 19
    • 41649097183 scopus 로고    scopus 로고
    • Kubinyi H., and Mueller G. (Eds), John Wiley
    • Mueller G. In: Kubinyi H., and Mueller G. (Eds). Chemogenomics in Drug Discovery (2004), John Wiley 19
    • (2004) Chemogenomics in Drug Discovery , pp. 19
    • Mueller, G.1
  • 25
    • 0030770085 scopus 로고    scopus 로고
    • for an improved procedure for the preparation of unhindered isoxazolyl-oxazolines, see:
    • for an improved procedure for the preparation of unhindered isoxazolyl-oxazolines, see:. Zhou P., Blubaum J.E., Burns C.T., and Natale N.R. Tetrahedron Lett. 38 (1997) 7019-7020
    • (1997) Tetrahedron Lett. , vol.38 , pp. 7019-7020
    • Zhou, P.1    Blubaum, J.E.2    Burns, C.T.3    Natale, N.R.4
  • 36
    • 33947465889 scopus 로고
    • This effect has been noted elsewhere:
    • This effect has been noted elsewhere:. House H.O. J. Am. Chem. Soc. 77 (1955) 3070
    • (1955) J. Am. Chem. Soc. , vol.77 , pp. 3070
    • House, H.O.1
  • 37
    • 41649119381 scopus 로고
    • Conversion of styrene oxide to phenyl acetaldehyde has been optimized
    • Conversion of styrene oxide to phenyl acetaldehyde has been optimized. Kim J.D., and Cha J.S. Taehan Hwahakhoe Chi 27 (1983) 73-75
    • (1983) Taehan Hwahakhoe Chi , vol.27 , pp. 73-75
    • Kim, J.D.1    Cha, J.S.2
  • 38
    • 0344549623 scopus 로고    scopus 로고
    • Unpublished result. No starting material or desired product is recovered on attempted oxidation with the Dess-Martin periodinane, whereas the secondary alcohol 3b is readily oxidized in high yields, see:
    • Unpublished result. No starting material or desired product is recovered on attempted oxidation with the Dess-Martin periodinane, whereas the secondary alcohol 3b is readily oxidized in high yields, see:. Nelson J.K., Burkhart D.J., McKenzie A., and Natale N.R. Synlett (2003) 2213-2215
    • (2003) Synlett , pp. 2213-2215
    • Nelson, J.K.1    Burkhart, D.J.2    McKenzie, A.3    Natale, N.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.