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Volumn 71, Issue 7, 1997, Pages 936-940

From sugar allyltins to chiral cyclopentadienes: Radical cyclization of highly oxygenated sugar-derived dienoaldehydes

Author keywords

Acyclic sugar derivatives; Chiral cyclopentanes; Radical cyclization

Indexed keywords


EID: 21744441928     PISSN: 01375083     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (16)
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    • Giese, B.1
  • 2
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    • Butterworth, London
    • Giese B., "Radicals in Organic Synthesis: Formation of a Carbon-Carbon Bond", Pergamon Press, New York (1986); Pereire M., Quintard J.-P. and Rahm A., "Tin in Organic Synthesis", Butterworth, London (1987) ; Curran, Synthesis; RajanBabu T. V., Acc. Chem. Res., 24, 139 (1991).
    • (1987) Tin in Organic Synthesis
    • Pereire, M.1    Quintard, J.-P.2    Rahm, A.3
  • 3
    • 30244529217 scopus 로고    scopus 로고
    • Giese B., "Radicals in Organic Synthesis: Formation of a Carbon-Carbon Bond", Pergamon Press, New York (1986); Pereire M., Quintard J.-P. and Rahm A., "Tin in Organic Synthesis", Butterworth, London (1987) ; Curran, Synthesis; RajanBabu T. V., Acc. Chem. Res., 24, 139 (1991).
    • Synthesis
    • Curran1
  • 4
    • 0010720585 scopus 로고
    • Giese B., "Radicals in Organic Synthesis: Formation of a Carbon-Carbon Bond", Pergamon Press, New York (1986); Pereire M., Quintard J.-P. and Rahm A., "Tin in Organic Synthesis", Butterworth, London (1987) ; Curran, Synthesis; RajanBabu T. V., Acc. Chem. Res., 24, 139 (1991).
    • (1991) Acc. Chem. Res. , vol.24 , pp. 139
    • RajanBabu, T.V.1
  • 7
    • 0027082531 scopus 로고
    • Ando O., Satake H., Itoi K., Sato A., Nakajima M., Takahashi S. and Haruyama H., J. Antibiot., 44, 1165 (1991); Kobayashi Y., Miyazaki H. and Shiozaki M., J. Am. Chem. Soc., 114, 10065 (1992).
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  • 8
    • 84986674947 scopus 로고
    • Helmuchen G., Krotz A., Neumann H.-P. and Ziegler M.L., Liebigs Ann., 1313 (1993); Gevorgyan V., Kadota I. and Yamamoto Y., Tetrahedron Lett., 34, 1313 (1993) Yoshikawa M., Yokokawa Y. Inoue Y., Yamaguchi S. and Murakami, N., Tetrahedron, 50, 9961 (1994).
    • (1993) Liebigs Ann. , pp. 1313
    • Helmuchen, G.1    Krotz, A.2    Neumann, H.-P.3    Ziegler, M.L.4
  • 9
    • 0027530713 scopus 로고
    • Helmuchen G., Krotz A., Neumann H.-P. and Ziegler M.L., Liebigs Ann., 1313 (1993); Gevorgyan V., Kadota I. and Yamamoto Y., Tetrahedron Lett., 34, 1313 (1993) Yoshikawa M., Yokokawa Y. Inoue Y., Yamaguchi S. and Murakami, N., Tetrahedron, 50, 9961 (1994).
    • (1993) Tetrahedron Lett. , vol.34 , pp. 1313
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  • 10
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    • Helmuchen G., Krotz A., Neumann H.-P. and Ziegler M.L., Liebigs Ann., 1313 (1993); Gevorgyan V., Kadota I. and Yamamoto Y., Tetrahedron Lett., 34, 1313 (1993) Yoshikawa M., Yokokawa Y. Inoue Y., Yamaguchi S. and Murakami, N., Tetrahedron, 50, 9961 (1994).
    • (1994) Tetrahedron , vol.50 , pp. 9961
    • Yoshikawa, M.1    Yokokawa, Y.2    Inoue, Y.3    Yamaguchi, S.4    Murakami, N.5
  • 12
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    • Agrofoglio L., Suhas E., Farese A., Condom R., Challand S.R., Earl R.A. and Guedj R., Tetrahedron, 50, 10611 (1994); Takahashi S., Inoue H. and Kuzuhara H., J. Carbohydr. Chem., 14, 273 (1995).
    • (1995) J. Carbohydr. Chem. , vol.14 , pp. 273
    • Takahashi, S.1    Inoue, H.2    Kuzuhara, H.3
  • 15
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    • and references therein
    • Hays D.S. and Fu G.C., J. Org. Chem., 61, 4 (1996) and references therein.
    • (1996) J. Org. Chem. , vol.61 , pp. 4
    • Hays, D.S.1    Fu, G.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.