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Volumn 38, Issue 47, 1997, Pages 8165-8168

Vinylogous sulfonates as radical acceptors for the stereoselective synthesis of cyclic ethers

Author keywords

[No Author keywords available]

Indexed keywords

ETHER DERIVATIVE; SULFONIC ACID DERIVATIVE; VINYL DERIVATIVE;

EID: 0030716171     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)10248-9     Document Type: Article
Times cited : (35)

References (33)
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    • (1982) Polyether Antibiotics , vol.1-2
    • Westley, J.W.1
  • 3
    • 0000359232 scopus 로고
    • Scheuer, P. J., Ed.; Academic Press: New York, Chapter 4
    • (c) Erickson, K. L. in Marine Natural Products, Scheuer, P. J., Ed.; Academic Press: New York, 1983, Vol. 5, Chapter 4, pp 131-257.
    • (1983) Marine Natural Products , vol.5 , pp. 131-257
    • Erickson, K.L.1
  • 4
    • 15844366864 scopus 로고
    • For recent reviews on cyclic ether syntheses, see: (a) Boivin, T. L. B. Tetrahedron 1987, 43, 3309.
    • (1987) Tetrahedron , vol.43 , pp. 3309
    • Boivin, T.L.B.1
  • 10
    • 0001216647 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon, Oxford
    • (d) Curran, D. P. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon, Oxford, 1992, Vol. 4, pp 715, 779.
    • (1992) Comprehensive Organic Synthesis , vol.4 , pp. 715
    • Curran, D.P.1
  • 11
    • 0001451085 scopus 로고    scopus 로고
    • and pertinent references therein
    • (e) Ryu, I.; Sonoda, N.; Curran, D. P. Chem. Rev. 1996, 96, 177 and pertinent references therein.
    • (1996) Chem. Rev. , vol.96 , pp. 177
    • Ryu, I.1    Sonoda, N.2    Curran, D.P.3
  • 12
    • 0028048103 scopus 로고
    • For some representative examples of cyclic ether synthesis via radical cyclizations see: (a) Burke, S. D.; Jung, W. -J. Tetrahedron Lett. 1994, 35, 5837.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 5837
    • Burke, S.D.1    Jung, W.-J.2
  • 20
    • 0031033067 scopus 로고    scopus 로고
    • and pertinent references within these articles
    • (i) Engman, L.; Gupta, V. J. Org. Chem. 1997, 62, 157 and pertinent references within these articles.
    • (1997) J. Org. Chem. , vol.62 , pp. 157
    • Engman, L.1    Gupta, V.2
  • 24
    • 0030857706 scopus 로고    scopus 로고
    • and pertinent references within these articles
    • (d) Evans, P. A.; Roseman, J. D. Tetrahedron Lett. 1997, 38, 5249 and pertinent references within these articles.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5249
    • Evans, P.A.1    Roseman, J.D.2
  • 25
    • 85036684659 scopus 로고    scopus 로고
    • note
    • 7 Chemical equations presented.
  • 27
    • 0001289004 scopus 로고
    • For a recent review on this reagent, see: Chatgilialoglu, C. Chem. Rev. 1995, 60, 3826.
    • (1995) Chem. Rev. , vol.60 , pp. 3826
    • Chatgilialoglu, C.1
  • 30
  • 32
    • 33947087440 scopus 로고
    • The LUMO of a vinyl sulfone and a vinyl ether are known to have larger coefficients at the β-and α-carbons respectively, thus reinforcing each other in a β-alkoxy vinyl sulfone. See: (a) Sims, J.; Houk, K. N. J. Am. Chem. Soc. 1973, 95, 5798.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 5798
    • Sims, J.1    Houk, K.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.