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1
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33748539998
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For comprehensive reviews on calixarenes see:
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For comprehensive reviews on calixarenes see:. Böhmer V. Angew. Chem., Int. Ed. Engl. 34 (1995) 713-745
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(1995)
Angew. Chem., Int. Ed. Engl.
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Böhmer, V.1
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4
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0004287470
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Asfari Z., Böhmer V., Harrowfield J., and Vicens J. (Eds), Kluwer, Dordrecht
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In: Asfari Z., Böhmer V., Harrowfield J., and Vicens J. (Eds). Calixarenes 2001 (2001), Kluwer, Dordrecht
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(2001)
Calixarenes 2001
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5
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0345736841
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In The, Rappoport, Z, Ed, Wiley: Chichester, UK, Chapter 19, pp
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Böhmer, V. In The Chemistry of Phenols; Rappoport, Z., Ed.; Wiley: Chichester, UK, 2003; Chapter 19, pp 1369-1454.
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(2003)
Chemistry of Phenols
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Böhmer, V.1
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6
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84892021501
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Vicens J., and Harrowfield J. (Eds), Springer, Dordrecht
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In: Vicens J., and Harrowfield J. (Eds). Calixarenes in the Nanoworld (2007), Springer, Dordrecht
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(2007)
Calixarenes in the Nanoworld
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7
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50249151074
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Royal Society of Chemistry, Cambridge, UK pp 25-26 and following chapters
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Gutsche C.D. Calixarenes, an Introduction (2008), Royal Society of Chemistry, Cambridge, UK pp 25-26 and following chapters
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(2008)
Calixarenes, an Introduction
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Gutsche, C.D.1
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9
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26844481422
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4f For general reviews see Ref. 1, while for representative or recent examples, see:
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4f For general reviews see Ref. 1, while for representative or recent examples, see:. Shinkai S., Koreishi H., Ueda K., Arimura T., and Manabe O. J. Am. Chem. Soc. 109 (1987) 6371-6376
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(1987)
J. Am. Chem. Soc.
, vol.109
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Shinkai, S.1
Koreishi, H.2
Ueda, K.3
Arimura, T.4
Manabe, O.5
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11
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0000529839
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Verboom W., Durie A., Egberink R.J.M., Asfari Z., and Reinhoudt D.N. J. Org. Chem. 57 (1992) 1313-1316
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(1992)
J. Org. Chem.
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Verboom, W.1
Durie, A.2
Egberink, R.J.M.3
Asfari, Z.4
Reinhoudt, D.N.5
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13
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33751155285
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Arduini A., Fanni S., Manfredi G., Pochini A., Ungaro R., Sicuri A.R., and Ugozzoli F. J. Org. Chem. 60 (1995) 1448-1453
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(1995)
J. Org. Chem.
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Arduini, A.1
Fanni, S.2
Manfredi, G.3
Pochini, A.4
Ungaro, R.5
Sicuri, A.R.6
Ugozzoli, F.7
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14
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0027370866
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Casnati A., Ting Y., Berti D., Fabbi M., Pochini A., Ungaro R., Sciotto D., and Lombardo G.G. Tetrahedron 49 (1993) 9815-9822
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(1993)
Tetrahedron
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Casnati, A.1
Ting, Y.2
Berti, D.3
Fabbi, M.4
Pochini, A.5
Ungaro, R.6
Sciotto, D.7
Lombardo, G.G.8
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17
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0000285995
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Almi M., Arduini A., Casnati A., Pochini A., and Ungaro R. Tetrahedron 45 (1989) 2177-2182
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(1989)
Tetrahedron
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Almi, M.1
Arduini, A.2
Casnati, A.3
Pochini, A.4
Ungaro, R.5
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20
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0032567396
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For a similar study on 4-bromo-2,6-di-tert-butylcyclohexa-2,5-dienone, see:
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For a similar study on 4-bromo-2,6-di-tert-butylcyclohexa-2,5-dienone, see:. Omura K. J. Org. Chem. 63 (1998) 10031-10034
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(1998)
J. Org. Chem.
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Omura, K.1
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22
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0001616005
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Swenton J.S., Callinan A., Chen Y., Rohde J.L., Kerns M.L., and Morrow G.L. J. Org. Chem. 61 (1996) 1267-1274
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(1996)
J. Org. Chem.
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Swenton, J.S.1
Callinan, A.2
Chen, Y.3
Rohde, J.L.4
Kerns, M.L.5
Morrow, G.L.6
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31
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66949167836
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note
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See Supplementary data for additional details.
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32
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66949179129
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note
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In addition to 3a and 4a, tripropoxy-p-tert-butylcalix[4]arene and tripropoxycalix[4]monoquinone were also isolated in 35% and 5% yield, respectively.
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33
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0000185077
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It is well known that 2,5-cyclohexadienone derivatives with two groups in position 4 undergo 1,2-migration of one of these groups (the dienone-phenol rearrangement) to afford phenolic compounds. For a review, see:
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It is well known that 2,5-cyclohexadienone derivatives with two groups in position 4 undergo 1,2-migration of one of these groups (the dienone-phenol rearrangement) to afford phenolic compounds. For a review, see:. Miller B. Acc. Chem. Res. 8 (1975) 245-256
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(1975)
Acc. Chem. Res.
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, pp. 245-256
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Miller, B.1
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34
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66949174877
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Rappoport Z. (Ed), Wiley, Chichester, UK Chapter 11, and references therein
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Lukyanov S.M., and Koblik A.V. In: Rappoport Z. (Ed). The Chemistry of Phenols (2003), Wiley, Chichester, UK 806-816 Chapter 11, and references therein
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(2003)
The Chemistry of Phenols
, pp. 806-816
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Lukyanov, S.M.1
Koblik, A.V.2
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35
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66949167837
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For more recent examples, see:
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For more recent examples, see:. Chen Y., Reymond J.-L., and Lerner R.A. Angew. Chem., Int. Ed. Engl. 33 (1994) 1694-1696
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(1994)
Angew. Chem., Int. Ed. Engl.
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Chen, Y.1
Reymond, J.-L.2
Lerner, R.A.3
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41
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33751386348
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Notwithstanding the special interest for the inherent chirality of meta-substituted calix[4]arenes, functionalizations at the meta-position are relatively uncommon. For some representative examples, see:
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Notwithstanding the special interest for the inherent chirality of meta-substituted calix[4]arenes, functionalizations at the meta-position are relatively uncommon. For some representative examples, see:. Reddy P.A., and Gutsche C.D. J. Org. Chem. 58 (1993) 3245-3251
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(1993)
J. Org. Chem.
, vol.58
, pp. 3245-3251
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Reddy, P.A.1
Gutsche, C.D.2
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42
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0028924920
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Verboom W., Bodewes P.J., Essen G.V., Timmerman P., Hummer G.J.V., Harkema S., and Reinhoudt D.N. Tetrahedron 51 (1995) 499-512
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(1995)
Tetrahedron
, vol.51
, pp. 499-512
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Verboom, W.1
Bodewes, P.J.2
Essen, G.V.3
Timmerman, P.4
Hummer, G.J.V.5
Harkema, S.6
Reinhoudt, D.N.7
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43
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Mascal M., Warmuth R., Naven R.T., Edwards R.A., Hursthouse M.B., and Hibbs D.E. J. Chem. Soc., Perkin Trans. 1 (1999) 3435-3441
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(1999)
J. Chem. Soc., Perkin Trans. 1
, pp. 3435-3441
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Mascal, M.1
Warmuth, R.2
Naven, R.T.3
Edwards, R.A.4
Hursthouse, M.B.5
Hibbs, D.E.6
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45
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35948998795
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For very interesting examples of non-chromatographic resolution of inherently chiral meta-substituted calixarenes, see:
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For very interesting examples of non-chromatographic resolution of inherently chiral meta-substituted calixarenes, see:. Xu Z.-X., Zhang C., Zheng Q.-Y., Chen C.-F., and Huang Z.-T. Org. Lett. 9 (2007) 4447-4450
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(2007)
Org. Lett.
, vol.9
, pp. 4447-4450
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Xu, Z.-X.1
Zhang, C.2
Zheng, Q.-Y.3
Chen, C.-F.4
Huang, Z.-T.5
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46
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Xu Z.-X., Zhang C., Yang Y., Chen C.-F., and Huang Z.-T. Org. Lett. 10 (2008) 477-479
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(2008)
Org. Lett.
, vol.10
, pp. 477-479
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Xu, Z.-X.1
Zhang, C.2
Yang, Y.3
Chen, C.-F.4
Huang, Z.-T.5
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49
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0002640110
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Abramovitch R.A., Bartnik R., Cooper M., Dassanayake N.L., Hwang H.Y., Inbasekaran M.N., and Rusek G. J. Org. Chem. 47 (1982) 4817-4818
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J. Org. Chem.
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Abramovitch, R.A.1
Bartnik, R.2
Cooper, M.3
Dassanayake, N.L.4
Hwang, H.Y.5
Inbasekaran, M.N.6
Rusek, G.7
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50
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0000394955
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Abramovitch R.A., Alvernhe G., Bartnik R., Dassanayake N.L., Inbasekaran M.N., and Kato S. J. Am. Chem. Soc. 103 (1981) 4558-4565
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Abramovitch, R.A.1
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Inbasekaran, M.N.5
Kato, S.6
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