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Volumn 37, Issue 6, 1996, Pages 783-786

Intramolecular 4+3 cycloadditions. Vinylthionium ions from allylic alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKENE DERIVATIVE; THIOPHENE DERIVATIVE;

EID: 0030029669     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(95)02391-7     Document Type: Article
Times cited : (36)

References (42)
  • 1
    • 0001753657 scopus 로고
    • [4+3] cycloadditions
    • Trost, B.M.; Fleming, I. Eds.; Pergamon: Oxford, Chapter 5.1
    • For reviews of 4+3 cycloadditions, see: (a) Hosomi, A. and Tominaga, Y. (1991) [4+3] cycloadditions. In Comprehensive Organic Synthesis; Trost, B.M.; Fleming, I. Eds.; Pergamon: Oxford, Vol. 5, Chapter 5.1, pp 593-615. (b) Hoffmann, H.M.R. Angew. Chem. Intl. Ed. Engl. 1984, 23, 1. (c) Mann, J. Tetrahedron 1986, 42, 4611. (d) Noyori, R. and Hayakawa, Y. Org. React. 1983, 29, 163-344.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 593-615
    • Hosomi, A.1    Tominaga, Y.2
  • 2
    • 84985566399 scopus 로고
    • For reviews of 4+3 cycloadditions, see: (a) Hosomi, A. and Tominaga, Y. (1991) [4+3] cycloadditions. In Comprehensive Organic Synthesis; Trost, B.M.; Fleming, I. Eds.; Pergamon: Oxford, Vol. 5, Chapter 5.1, pp 593-615. (b) Hoffmann, H.M.R. Angew. Chem. Intl. Ed. Engl. 1984, 23, 1. (c) Mann, J. Tetrahedron 1986, 42, 4611. (d) Noyori, R. and Hayakawa, Y. Org. React. 1983, 29, 163-344.
    • (1984) Angew. Chem. Intl. Ed. Engl. , vol.23 , pp. 1
    • Hoffmann, H.M.R.1
  • 3
    • 0001523555 scopus 로고
    • For reviews of 4+3 cycloadditions, see: (a) Hosomi, A. and Tominaga, Y. (1991) [4+3] cycloadditions. In Comprehensive Organic Synthesis; Trost, B.M.; Fleming, I. Eds.; Pergamon: Oxford, Vol. 5, Chapter 5.1, pp 593-615. (b) Hoffmann, H.M.R. Angew. Chem. Intl. Ed. Engl. 1984, 23, 1. (c) Mann, J. Tetrahedron 1986, 42, 4611. (d) Noyori, R. and Hayakawa, Y. Org. React. 1983, 29, 163-344.
    • (1986) Tetrahedron , vol.42 , pp. 4611
    • Mann, J.1
  • 4
    • 0000400239 scopus 로고
    • For reviews of 4+3 cycloadditions, see: (a) Hosomi, A. and Tominaga, Y. (1991) [4+3] cycloadditions. In Comprehensive Organic Synthesis; Trost, B.M.; Fleming, I. Eds.; Pergamon: Oxford, Vol. 5, Chapter 5.1, pp 593-615. (b) Hoffmann, H.M.R. Angew. Chem. Intl. Ed. Engl. 1984, 23, 1. (c) Mann, J. Tetrahedron 1986, 42, 4611. (d) Noyori, R. and Hayakawa, Y. Org. React. 1983, 29, 163-344.
    • (1983) Org. React. , vol.29 , pp. 163-344
    • Noyori, R.1    Hayakawa, Y.2
  • 5
    • 0004136903 scopus 로고
    • Lautens, M., Ed.; JAI: Greenwich, in press
    • For a review of intramolecular 4+3 cycloadditions, see: Harmata, M. In Advances in Cycloaddition; Lautens, M., Ed.; JAI: Greenwich, 1995, Vol. 4, (in press).
    • (1995) Advances in Cycloaddition , vol.4
    • Harmata, M.1
  • 37
    • 85030013955 scopus 로고    scopus 로고
    • note
    • -1; F(000) = 642.92; Temperature = 23 + 1°; Final R = 0.035 for 2093 reflections with I>2σ(I).
  • 42
    • 85030003552 scopus 로고    scopus 로고
    • note
    • 13C NMR, IR and combustion analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.