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61349162745
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This report is part 133 of a series entitled The Chemistry of Indoles
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This report is part 133 of a series entitled The Chemistry of Indoles.
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6
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0000228416
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Nucleophilic substitution reactions were suggested in the following literatures:
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Nucleophilic substitution reactions were suggested in the following literatures:. Hermkens P.H.H., Plate R., Kruse C.G., Scheeren H.W., and Ottenheijm H.C.J. J. Org. Chem. 57 (1992) 3881
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(1992)
J. Org. Chem.
, vol.57
, pp. 3881
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Hermkens, P.H.H.1
Plate, R.2
Kruse, C.G.3
Scheeren, H.W.4
Ottenheijm, H.C.J.5
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7
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33751392279
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Becher J., Jfrgensen P.L., Pluta K., Krake N.J., and Hansen B.F. J. Org. Chem. 57 (1992) 2127
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(1992)
J. Org. Chem.
, vol.57
, pp. 2127
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Becher, J.1
Jfrgensen, P.L.2
Pluta, K.3
Krake, N.J.4
Hansen, B.F.5
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10
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37049108483
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Dalton L., Humphrey G.L., Cooper M.M., and Joule J.A. J. Chem. Soc., Perkin Trans. 1 (1983) 2417
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(1983)
J. Chem. Soc., Perkin Trans. 1
, pp. 2417
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Dalton, L.1
Humphrey, G.L.2
Cooper, M.M.3
Joule, J.A.4
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11
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37049097835
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Beal M.G., Ashcroft W.R., Cooper M.M., and Joule J.A. J. Chem. Soc., Perkin Trans. 1 (1982) 435
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(1982)
J. Chem. Soc., Perkin Trans. 1
, pp. 435
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Beal, M.G.1
Ashcroft, W.R.2
Cooper, M.M.3
Joule, J.A.4
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17
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0017697918
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Hino T., Endo M., Tonozuka M., Hashimoto Y., and Nakagawa M. Chem. Pharm. Bull. 25 (1977) 2350
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(1977)
Chem. Pharm. Bull.
, vol.25
, pp. 2350
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Hino, T.1
Endo, M.2
Tonozuka, M.3
Hashimoto, Y.4
Nakagawa, M.5
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21
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0036096658
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Katritzky A.R. (Ed), Elsevier Science, USA
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Somei M. In: Katritzky A.R. (Ed). Advances in Heterocyclic Chemistry Vol. 82 (2002), Elsevier Science, USA 101-155
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(2002)
Advances in Heterocyclic Chemistry
, vol.82
, pp. 101-155
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Somei, M.1
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61349203667
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note
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3 nitrogen on the departure of the hydroxy group. Consequently nucleophilic substitution reaction at the 5- and/or other positions of indole nucleus becomes possible. For more details: M. Somei, "Topics in Heterocyclic Chemistry", Vol. 6, ed. by S. Eguchi, Springer-Verlag, Berlin, 2006, pp. 77-111.{A figure is presented}
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26
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33947306110
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Somei M., Noguchi K., Yoshino K., Mori K., Asada M., Yamada F., Tanaka Y., Shigenobu K., and Koike K. Heterocycles 69 (2006) 259
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(2006)
Heterocycles
, vol.69
, pp. 259
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Somei, M.1
Noguchi, K.2
Yoshino, K.3
Mori, K.4
Asada, M.5
Yamada, F.6
Tanaka, Y.7
Shigenobu, K.8
Koike, K.9
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0000466116
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Takayama H., Seki N., Kitajima M., Aimi N., Seki H., and Sakai S. Heterocycles 33 (1992) 121
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(1992)
Heterocycles
, vol.33
, pp. 121
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Takayama, H.1
Seki, N.2
Kitajima, M.3
Aimi, N.4
Seki, H.5
Sakai, S.6
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61349088388
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3-hexane)
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Noguchi K. (Ed), Kanazawa University March
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3-hexane). In: Noguchi K. (Ed). Master Thesis (2000), Kanazawa University March
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(2000)
Master Thesis
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61349202617
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All measurements were made on a Rigaku/MSC Mercury diffract meter with graphite monochromated Mo-Kα radiation. All calculations were performed using the teXsan package. The structure was solved by a direct method (SIR).12 The non-hydrogen atoms were refined anisotropically. Hydrogen atoms were included but not refined. Detailed crystal data would be reported elsewhere in due course
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12 The non-hydrogen atoms were refined anisotropically. Hydrogen atoms were included but not refined. Detailed crystal data would be reported elsewhere in due course.
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30
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61349093885
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mp 167-169°C (decomp., colorless prisms, recrystallized from McOH). b) pale yellow oil. c) pale yellow oil. d) pale yellow oil. e) pale yellow oil. f) pale yellow oil.
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a) mp 167-169°C (decomp., colorless prisms, recrystallized from McOH). b) pale yellow oil. c) pale yellow oil. d) pale yellow oil. e) pale yellow oil. f) pale yellow oil.
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31
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61349141688
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teXsan: Crystal Structure Analysis Package, Molecular Structure Corporation, 1985 & 1999.
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teXsan: Crystal Structure Analysis Package, Molecular Structure Corporation, 1985 & 1999.
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32
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84992249157
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Burla M.C., Camalli M., Cascarano M., Giacovazzo C., Guagliardi A., and Polidori G. J. Appl. Cryst. 27 (1994) 435
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(1994)
J. Appl. Cryst.
, vol.27
, pp. 435
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Burla, M.C.1
Camalli, M.2
Cascarano, M.3
Giacovazzo, C.4
Guagliardi, A.5
Polidori, G.6
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