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Volumn 15, Issue 25, 1996, Pages 5335-5341

Synthesis and reactions of neutral hypercoordinate allylsilicon compounds having a tropolonato ligand

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EID: 0001454484     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om960557g     Document Type: Article
Times cited : (22)

References (44)
  • 1
    • 0004095340 scopus 로고
    • Butterworth: London
    • For reviews, see: (a) Colvin, E. W.; Silicon in Organic Synthesis; Butterworth: London, 1981. (b) Weber W. P. Silicon Reagents for Organic Synthesis; Springer: New York, 1982. (c) Schinzer, D. Synthesis 1988, 263. (d) Chuit, C.; Corriu, R. J. P.; Reye, C.; Young, J. C. Chem. Rev. 1993, 93, 1371. (e) Masse, C. E.; Panek, J. S. Chem. Rev. 1995, 95, 1293.
    • (1981) Silicon in Organic Synthesis
    • Colvin, E.W.1
  • 2
    • 0004064176 scopus 로고
    • Springer: New York
    • For reviews, see: (a) Colvin, E. W.; Silicon in Organic Synthesis; Butterworth: London, 1981. (b) Weber W. P. Silicon Reagents for Organic Synthesis; Springer: New York, 1982. (c) Schinzer, D. Synthesis 1988, 263. (d) Chuit, C.; Corriu, R. J. P.; Reye, C.; Young, J. C. Chem. Rev. 1993, 93, 1371. (e) Masse, C. E.; Panek, J. S. Chem. Rev. 1995, 95, 1293.
    • (1982) Silicon Reagents for Organic Synthesis
    • Weber, W.P.1
  • 3
    • 85082709521 scopus 로고
    • For reviews, see: (a) Colvin, E. W.; Silicon in Organic Synthesis; Butterworth: London, 1981. (b) Weber W. P. Silicon Reagents for Organic Synthesis; Springer: New York, 1982. (c) Schinzer, D. Synthesis 1988, 263. (d) Chuit, C.; Corriu, R. J. P.; Reye, C.; Young, J. C. Chem. Rev. 1993, 93, 1371. (e) Masse, C. E.; Panek, J. S. Chem. Rev. 1995, 95, 1293.
    • (1988) Synthesis , pp. 263
    • Schinzer, D.1
  • 4
    • 0001214450 scopus 로고
    • For reviews, see: (a) Colvin, E. W.; Silicon in Organic Synthesis; Butterworth: London, 1981. (b) Weber W. P. Silicon Reagents for Organic Synthesis; Springer: New York, 1982. (c) Schinzer, D. Synthesis 1988, 263. (d) Chuit, C.; Corriu, R. J. P.; Reye, C.; Young, J. C. Chem. Rev. 1993, 93, 1371. (e) Masse, C. E.; Panek, J. S. Chem. Rev. 1995, 95, 1293.
    • (1993) Chem. Rev. , vol.93 , pp. 1371
    • Chuit, C.1    Corriu, R.J.P.2    Reye, C.3    Young, J.C.4
  • 5
    • 0343778881 scopus 로고
    • For reviews, see: (a) Colvin, E. W.; Silicon in Organic Synthesis; Butterworth: London, 1981. (b) Weber W. P. Silicon Reagents for Organic Synthesis; Springer: New York, 1982. (c) Schinzer, D. Synthesis 1988, 263. (d) Chuit, C.; Corriu, R. J. P.; Reye, C.; Young, J. C. Chem. Rev. 1993, 93, 1371. (e) Masse, C. E.; Panek, J. S. Chem. Rev. 1995, 95, 1293.
    • (1995) Chem. Rev. , vol.95 , pp. 1293
    • Masse, C.E.1    Panek, J.S.2
  • 16
    • 0001796486 scopus 로고
    • and references therein
    • (e) Sakurai, H. Synlett 1989, 1 and references therein.
    • (1989) Synlett , pp. 1
    • Sakurai, H.1
  • 25
    • 0002893470 scopus 로고
    • w = 0.067. All calculations were performed by an ACOS-2200 computer at Tohoku University with the applied library program UNICS III (Sakurai, T.; Kobayashi, K. Rikagaku Kenkyusho Hokoku 1979, 55, 69).
    • (1979) Rikagaku Kenkyusho Hokoku , vol.55 , pp. 69
    • Sakurai, T.1    Kobayashi, K.2
  • 38
    • 2542437972 scopus 로고
    • A number of allylation of tropolone are reported: (a) Nozoe, T.; Mukai, T.; Murata, I. Proc. Jpn. Acad. 1953, 29, 169. (b) Nozoe, T.; Mukai, T.; Asao, T. Bull. Chem. Soc. Jpn. 1960, 33, 1452. (c) Goldshmidt, Z.; Antebi, S. Tetrahedron Lett. 1978, 1225.
    • (1953) Proc. Jpn. Acad. , vol.29 , pp. 169
    • Nozoe, T.1    Mukai, T.2    Murata, I.3
  • 39
    • 0000023722 scopus 로고
    • A number of allylation of tropolone are reported: (a) Nozoe, T.; Mukai, T.; Murata, I. Proc. Jpn. Acad. 1953, 29, 169. (b) Nozoe, T.; Mukai, T.; Asao, T. Bull. Chem. Soc. Jpn. 1960, 33, 1452. (c) Goldshmidt, Z.; Antebi, S. Tetrahedron Lett. 1978, 1225.
    • (1960) Bull. Chem. Soc. Jpn. , vol.33 , pp. 1452
    • Nozoe, T.1    Mukai, T.2    Asao, T.3
  • 40
    • 0006014728 scopus 로고
    • A number of allylation of tropolone are reported: (a) Nozoe, T.; Mukai, T.; Murata, I. Proc. Jpn. Acad. 1953, 29, 169. (b) Nozoe, T.; Mukai, T.; Asao, T. Bull. Chem. Soc. Jpn. 1960, 33, 1452. (c) Goldshmidt, Z.; Antebi, S. Tetrahedron Lett. 1978, 1225.
    • (1978) Tetrahedron Lett. , pp. 1225
    • Goldshmidt, Z.1    Antebi, S.2


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