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1
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0000033877
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Calixarenes
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Reviews:. Stoddart J.F. (Ed), The Royal Society of Chemistry, Cambridge
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Reviews:. Gutsche C.D. Calixarenes. In: Stoddart J.F. (Ed). Monographs in Supramolecular Chemistry (1989), The Royal Society of Chemistry, Cambridge
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(1989)
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Gutsche, C.D.1
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3
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0003277099
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Calixarenes Revisited
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Stoddart J.F. (Ed), The Royal Society of Chemistry, Cambridge
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Gutsche C.D. Calixarenes Revisited. In: Stoddart J.F. (Ed). Monographs in Supramolecular Chemistry (1998), The Royal Society of Chemistry, Cambridge
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(1998)
Monographs in Supramolecular Chemistry
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Gutsche, C.D.1
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4
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0004266535
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Mandolini L., and Ungaro R. (Eds), Imperial College Press, London
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In: Mandolini L., and Ungaro R. (Eds). Calixarenes in Action (2000), Imperial College Press, London
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(2000)
Calixarenes in Action
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5
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0004287470
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Asfari Z., Böhmer V., Harrowfield J.M., and Vicens J. (Eds), Kluwer Academic, Dordrecht
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In: Asfari Z., Böhmer V., Harrowfield J.M., and Vicens J. (Eds). Calixarenes 2001 (2001), Kluwer Academic, Dordrecht
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(2001)
Calixarenes 2001
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6
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33751553183
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For iodination of the upper rim of calixarenes, see:
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For iodination of the upper rim of calixarenes, see:. van Loon J.-D., Arduini A., Coppi L., Verboom W., Pochini A., Ungaro R., Harkema S., and Reinhoudt D.N. J. Org. Chem. 55 (1990) 5639
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van Loon, J.-D.1
Arduini, A.2
Coppi, L.3
Verboom, W.4
Pochini, A.5
Ungaro, R.6
Harkema, S.7
Reinhoudt, D.N.8
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7
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0025309222
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Arduini A., Pochini A., Rizzi A., Sicuri A.R., and Ungaro R. Tetrahedron Lett. 31 (1990) 4653
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(1990)
Tetrahedron Lett.
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, pp. 4653
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Arduini, A.1
Pochini, A.2
Rizzi, A.3
Sicuri, A.R.4
Ungaro, R.5
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8
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85088085049
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Timmerman P., Verboom W., Reinhoudt D.N., Arduini A., Grandi S., Sicuri A.R., Pochini A., and Ungaro R. Synthesis (1994) 185
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(1994)
Synthesis
, pp. 185
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Timmerman, P.1
Verboom, W.2
Reinhoudt, D.N.3
Arduini, A.4
Grandi, S.5
Sicuri, A.R.6
Pochini, A.7
Ungaro, R.8
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9
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0001405867
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Aruduini A., McGregor W.M., Pochini A., Secchi A., Ugozzoli F., and Ungaro R. J. Org. Chem. 61 (1996) 6881
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Aruduini, A.1
McGregor, W.M.2
Pochini, A.3
Secchi, A.4
Ugozzoli, F.5
Ungaro, R.6
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10
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85045534276
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Arduini A., McGregor W.M., Paganuzzi D., Pochini A., Secchi A., Ugozzoli F., and Ungaro R. J. Chem. Soc., Perkin Trans. 2 (1996) 839
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(1996)
J. Chem. Soc., Perkin Trans. 2
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Arduini, A.1
McGregor, W.M.2
Paganuzzi, D.3
Pochini, A.4
Secchi, A.5
Ugozzoli, F.6
Ungaro, R.7
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13
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0030910727
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van Wageningen A.M.A., Timmerman P., van Duynhoven J.P.M., Verboom W., van Veggel F.C.J.M., and Reinhoudt D.N. Chem. Eur. J. 3 (1997) 639
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van Wageningen, A.M.A.1
Timmerman, P.2
van Duynhoven, J.P.M.3
Verboom, W.4
van Veggel, F.C.J.M.5
Reinhoudt, D.N.6
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16
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34250835413
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note
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It was also reported that a diazonium salt of monoaminocalix[5]arene on treatment with tetrabutylammonium iodide in chloroform afforded a practically unisolable mixture of monochloro- and monoiodocalix[5]arene. See Ref. 5.
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18
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0001228599
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For transformation of the hydroxy group of calixarenes into other functions, see:
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For transformation of the hydroxy group of calixarenes into other functions, see:. Gibbs C.G., Sujeeth P.K., Rogers J.S., Stanley G.G., Krawiec M., Watson W.H., and Gutsche C.D. J. Org. Chem. 60 (1995) 8394
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(1995)
J. Org. Chem.
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, pp. 8394
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Gibbs, C.G.1
Sujeeth, P.K.2
Rogers, J.S.3
Stanley, G.G.4
Krawiec, M.5
Watson, W.H.6
Gutsche, C.D.7
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21
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33846317803
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and references cited therein
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Morohashi N., Narumi F., Iki N., Hattori T., and Miyano S. Chem. Rev. 106 (2006) 5291 and references cited therein
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(2006)
Chem. Rev.
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, pp. 5291
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Morohashi, N.1
Narumi, F.2
Iki, N.3
Hattori, T.4
Miyano, S.5
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22
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0000359287
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NAr reaction, see:
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NAr reaction, see:. Hattori T., Hotta H., Suzuki T., and Miyano S. Bull. Chem. Soc. Jpn. 66 (1993) 613
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(1993)
Bull. Chem. Soc. Jpn.
, vol.66
, pp. 613
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Hattori, T.1
Hotta, H.2
Suzuki, T.3
Miyano, S.4
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23
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0000097819
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Hattori T., Suzuki T., Hayashizaka N., Koike N., and Miyano S. Bull. Chem. Soc. Jpn. 66 (1993) 3034
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(1993)
Bull. Chem. Soc. Jpn.
, vol.66
, pp. 3034
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Hattori, T.1
Suzuki, T.2
Hayashizaka, N.3
Koike, N.4
Miyano, S.5
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25
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33749088959
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Hattori T., Suzuki M., Tomita N., Takeda A., and Miyano S. J. Chem. Soc., Perkin Trans. 1 (1997) 1117
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(1997)
J. Chem. Soc., Perkin Trans. 1
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Hattori, T.1
Suzuki, M.2
Tomita, N.3
Takeda, A.4
Miyano, S.5
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26
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33748726440
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Hattori T., Takeda A., Suzuki K., Koike N., Koshiishi E., and Miyano S. J. Chem. Soc., Perkin Trans. 1 (1998) 3661
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(1998)
J. Chem. Soc., Perkin Trans. 1
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Hattori, T.1
Takeda, A.2
Suzuki, K.3
Koike, N.4
Koshiishi, E.5
Miyano, S.6
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27
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0037459675
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Hattori T., Shimazumi Y., Goto H., Yamabe O., Morohashi N., Kawai W., and Miyano S. J. Org. Chem. 68 (2003) 2099
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(2003)
J. Org. Chem.
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Hattori, T.1
Shimazumi, Y.2
Goto, H.3
Yamabe, O.4
Morohashi, N.5
Kawai, W.6
Miyano, S.7
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28
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0037459715
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For stereoisomers of sulfinylcalix[4]arene, see:
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For stereoisomers of sulfinylcalix[4]arene, see:. Morohashi N., Katagiri H., Iki N., Yamane Y., Kabuto C., Hattori T., and Miyano S. J. Org. Chem. 68 (2003) 2324
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(2003)
J. Org. Chem.
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, pp. 2324
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Morohashi, N.1
Katagiri, H.2
Iki, N.3
Yamane, Y.4
Kabuto, C.5
Hattori, T.6
Miyano, S.7
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29
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0035977622
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Katagiri H., Iki N., Hattori T., Kabuto C., and Miyano S. J. Am. Chem. Soc. 123 (2001) 779
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(2001)
J. Am. Chem. Soc.
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Katagiri, H.1
Iki, N.2
Hattori, T.3
Kabuto, C.4
Miyano, S.5
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31
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85046913734
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Katagiri H., Iki N., Matsunaga Y., Kabuto C., and Miyano S. Chem. Commun. (2002) 2080
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(2002)
Chem. Commun.
, pp. 2080
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Katagiri, H.1
Iki, N.2
Matsunaga, Y.3
Kabuto, C.4
Miyano, S.5
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36
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34250857223
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note
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+).
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37
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34250793117
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note
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4 and evaporated to leave a residue, which was chromatographed on silica gel with chloroform-hexane (1:2) as an eluent to give iodide 14 (57.1 mg, 55%).
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38
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34250830039
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note
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+).
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39
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34250823287
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note
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2 = 0.0438 (all data). Crystallographic data reported in this Letter have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication Nos. CCDC 644542 and 644543.
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