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Volumn 41, Issue 3, 2000, Pages 321-324

First synthesis of 1,4-bis(acylsilanes)

Author keywords

[No Author keywords available]

Indexed keywords

SILANE DERIVATIVE;

EID: 0034650822     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)02083-3     Document Type: Article
Times cited : (18)

References (24)
  • 6
    • 0001342637 scopus 로고
    • Carey, F. A.; Court, A. S. J. Org. Chem. 1972, 37, 1926-1929. Schlecker, R.; Henkel, U.; Seebach, D. Chem. Ber. 1977, 110, 2880-2904.
    • (1972) J. Org. Chem. , vol.37 , pp. 1926-1929
    • Carey, F.A.1    Court, A.S.2
  • 7
    • 84948286785 scopus 로고
    • Carey, F. A.; Court, A. S. J. Org. Chem. 1972, 37, 1926-1929. Schlecker, R.; Henkel, U.; Seebach, D. Chem. Ber. 1977, 110, 2880-2904.
    • (1977) Chem. Ber. , vol.110 , pp. 2880-2904
    • Schlecker, R.1    Henkel, U.2    Seebach, D.3
  • 8
    • 0342612298 scopus 로고    scopus 로고
    • 13C NMR)
    • 13C NMR).
  • 10
    • 0002639647 scopus 로고
    • Corey, E. J.; Seebach, D. Angew. Chem., Int. Ed. Engl. 1965, 4, 1075-1077. Seebach, D. Synthesis 1969, 17-36.
    • (1969) Synthesis , pp. 17-36
    • Seebach, D.1
  • 16
    • 0000315016 scopus 로고
    • The 1,2-bis(triflates) have been prepared according to the general procedure described by
    • The 1,2-bis(triflates) have been prepared according to the general procedure described by: Salomon, M. F.; Salomon, R. G. J. Am. Chem. Soc. 1979, 101, 4290-4299.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 4290-4299
    • Salomon, M.F.1    Salomon, R.G.2
  • 17
    • 0343482256 scopus 로고    scopus 로고
    • 4), 46.5 (CH)
    • 4), 46.5 (CH).
  • 18
    • 0342612297 scopus 로고    scopus 로고
    • Compound 3b was accompanied by a small amount of (2-prop-2-enyl[1,3]dithian-2-yl)trimethylsilane
    • Compound 3b was accompanied by a small amount of (2-prop-2-enyl[1,3]dithian-2-yl)trimethylsilane.
  • 19
  • 20
    • 33646850080 scopus 로고
    • Seebach, D.; Jones, N. R.; Corey, E. J. J. Org. Chem. 1968, 33, 300-305. Sudweeks, W. B.; Broadbent, H. S. J. Org. Chem. 1975, 40, 1131-1136.
    • (1975) J. Org. Chem. , vol.40 , pp. 1131-1136
    • Sudweeks, W.B.1    Broadbent, H.S.2
  • 21
    • 0343482255 scopus 로고    scopus 로고
    • 2), 244.2 (CO)
    • 2), 244.2 (CO).
  • 22
    • 34250562050 scopus 로고
    • 4). The furane 6a has been already prepared in low yield starting from furane and trimethylsilyl chloride
    • 4). The furane 6a has been already prepared in low yield starting from furane and trimethylsilyl chloride: Lukevits, E. Ya.; Voronkov, M. G. Khim. Geterotsikl. Soedin. 1965, 1, 19-31. Carman, C. S.; Koser, G. F. J. Org. Chem. 1983, 48, 2534-2539.
    • (1965) Khim. Geterotsikl. Soedin. , vol.1 , pp. 19-31
    • Lukevits, E.ya.1    Voronkov, M.G.2
  • 23
    • 0000108754 scopus 로고
    • 4). The furane 6a has been already prepared in low yield starting from furane and trimethylsilyl chloride: Lukevits, E. Ya.; Voronkov, M. G. Khim. Geterotsikl. Soedin. 1965, 1, 19-31. Carman, C. S.; Koser, G. F. J. Org. Chem. 1983, 48, 2534-2539.
    • (1983) J. Org. Chem. , vol.48 , pp. 2534-2539
    • Carman, C.S.1    Koser, G.F.2
  • 24
    • 0342612296 scopus 로고    scopus 로고
    • 4)
    • 4).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.