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Volumn 37, Issue 20, 1996, Pages 3581-3584

Oxygenation of alkenes with t-BuOOH catalysed by β-cyclodextrin borate

Author keywords

[No Author keywords available]

Indexed keywords

ALKANOL; HYDROXYACID;

EID: 0029967211     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00627-2     Document Type: Article
Times cited : (7)

References (26)
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    • note
    • Even after repeated efforts satisfactory elemental analysis could not be obtained.
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    • note
    • 3 and their physical mixture show strong signals); DSC: 398, 422, 440 K.
  • 12
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    • note
    • 2)]
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    • Kropf, H.; Amirabadi, H. M.; Mosebach, M.; Torkler, A.; von Wallis, J. Synthesis, 1983, 587; Kropf, H.; Ball, M.; Schroder, H.; Witte, G. Tetrahedron, 1974, 30, 2943.
    • (1974) Tetrahedron , vol.30 , pp. 2943
    • Kropf, H.1    Ball, M.2    Schroder, H.3    Witte, G.4
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    • note
    • 3 are essential for the reaction.
  • 17
    • 85030209704 scopus 로고
    • Ger. Offen., 2440951, 1975
    • Gaylord, N. G. Ger. Offen., 2440951, 1975; Chem. Abstr. 1975, 83, 11196h; Mageli, M. L.; Swarts, W. A. Ger. Offen. 2631911, 1977; Chem. Abstr. 1977, 86, 156821e; Haitt, R. In, Organic Peroxides, Swern, D. Ed.; John Wiley & Sons: New York, 1972; Vol. III, Chapter 1.
    • (1975) Chem. Abstr. , vol.83
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    • Ger. Offen. 2631911, 1977
    • Gaylord, N. G. Ger. Offen., 2440951, 1975; Chem. Abstr. 1975, 83, 11196h; Mageli, M. L.; Swarts, W. A. Ger. Offen. 2631911, 1977; Chem. Abstr. 1977, 86, 156821e; Haitt, R. In, Organic Peroxides, Swern, D. Ed.; John Wiley & Sons: New York, 1972; Vol. III, Chapter 1.
    • (1977) Chem. Abstr. , vol.86
    • Mageli, M.L.1    Swarts, W.A.2
  • 19
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    • Swern, D. Ed.; John Wiley & Sons: New York, Chapter 1
    • Gaylord, N. G. Ger. Offen., 2440951, 1975; Chem. Abstr. 1975, 83, 11196h; Mageli, M. L.; Swarts, W. A. Ger. Offen. 2631911, 1977; Chem. Abstr. 1977, 86, 156821e; Haitt, R. In, Organic Peroxides, Swern, D. Ed.; John Wiley & Sons: New York, 1972; Vol. III, Chapter 1.
    • (1972) Organic Peroxides , vol.3
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    • Higuchi, Y.; Matsuyama, K.; Komai, T. Bull. Chem. Soc. Jpn. 1988, 61, 1821; Barusch, M. R.; Payne, J. Q. J. Am. Chem. Soc. 1953, 75, 1987; Richardson, W. H.; Smith, R. S. J. Org. Chem. 1968, 33, 3882.
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    • Higuchi, Y.; Matsuyama, K.; Komai, T. Bull. Chem. Soc. Jpn. 1988, 61, 1821; Barusch, M. R.; Payne, J. Q. J. Am. Chem. Soc. 1953, 75, 1987; Richardson, W. H.; Smith, R. S. J. Org. Chem. 1968, 33, 3882.
    • (1953) J. Am. Chem. Soc. , vol.75 , pp. 1987
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    • note
    • 3CN, upto 10% of the corresponding epoxide was produced along with the other products. The authentic epoxide when treated under identical conditions yielded the dioxy alcohols (9a + 9b).
  • 24
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    • Duchene, D.; Wouessidjewe, D. J. Coord. Chem., 1992, 27, 223; Downing, D. D.; Hedges, A. R.; Reed, G. A. Eds.; The Sixth International Cyclodextrin Symposium. Book of Abstracts, pp. L-37, L-47, P-64, American Maize; Chicago, 1992.
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    • Duchene, D.1    Wouessidjewe, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.