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(a) The term tectons for building blocks in crystal engineering was first suggested by Wuest et al. in: Simard M., Su D., Wuest J.D. J. Am. Chem. Soc. 113:1991;4696; (b) Whitesides G.M., Mathias J.-P., Seto C.T. Science. 1991;254; (c) Lehn J.-M., Mascal M., DeCain A., Fischer J. J. Chem. Soc., Chem. Commun. 1990;479; (d) Aakeröy C.B., Beatty A.M., Helfrich B.A. Angew. Chem., Int. Ed. 40:2001;3240; (e) Bhyrappa P., Wilson S.R., Suslick K.S. J. Am. Chem. Soc. 119:1997;8492.
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(a) The term tectons for building blocks in crystal engineering was first suggested by Wuest et al. in: Simard M., Su D., Wuest J.D. J. Am. Chem. Soc. 113:1991;4696; (b) Whitesides G.M., Mathias J.-P., Seto C.T. Science. 1991;254; (c) Lehn J.-M., Mascal M., DeCain A., Fischer J. J. Chem. Soc., Chem. Commun. 1990;479; (d) Aakeröy C.B., Beatty A.M., Helfrich B.A. Angew. Chem., Int. Ed. 40:2001;3240; (e) Bhyrappa P., Wilson S.R., Suslick K.S. J. Am. Chem. Soc. 119:1997;8492.
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Lehn, J.-M.1
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0035801532
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(a) The term tectons for building blocks in crystal engineering was first suggested by Wuest et al. in: Simard M., Su D., Wuest J.D. J. Am. Chem. Soc. 113:1991;4696; (b) Whitesides G.M., Mathias J.-P., Seto C.T. Science. 1991;254; (c) Lehn J.-M., Mascal M., DeCain A., Fischer J. J. Chem. Soc., Chem. Commun. 1990;479; (d) Aakeröy C.B., Beatty A.M., Helfrich B.A. Angew. Chem., Int. Ed. 40:2001;3240; (e) Bhyrappa P., Wilson S.R., Suslick K.S. J. Am. Chem. Soc. 119:1997;8492.
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Aakeröy, C.B.1
Beatty, A.M.2
Helfrich, B.A.3
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21
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0030833305
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(a) The term tectons for building blocks in crystal engineering was first suggested by Wuest et al. in: Simard M., Su D., Wuest J.D. J. Am. Chem. Soc. 113:1991;4696; (b) Whitesides G.M., Mathias J.-P., Seto C.T. Science. 1991;254; (c) Lehn J.-M., Mascal M., DeCain A., Fischer J. J. Chem. Soc., Chem. Commun. 1990;479; (d) Aakeröy C.B., Beatty A.M., Helfrich B.A. Angew. Chem., Int. Ed. 40:2001;3240; (e) Bhyrappa P., Wilson S.R., Suslick K.S. J. Am. Chem. Soc. 119:1997;8492.
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Bhyrappa, P.1
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31
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33751134815
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For the synthesis of a structurally close analogue of
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For the synthesis of a structurally close analogue of 1 and 2 using an alternate Suzuki coupling approach, See: Chen T.-S., Gantzel P., Siegel J.S., Baldridge K.K., English R.B., Ho D.M. Angew. Chem., Int. Ed. 34:1995;2657.
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Chen, T.-S.1
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Baldridge, K.K.4
English, R.B.5
Ho, D.M.6
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32
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85031082866
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note
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3): δ 141.8, 141.5, 138.6, 138.3, 137.9, 136.0, 131.9, 130.0, 129.9, 127.2, 125.6, 74.6, 58.2.
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33
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85031077106
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+): 675.25354. Found: 675.25283
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+): 675.25354. Found: 675.25283.
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35
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85031072076
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+): 787.23319. Found 787.23231
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+): 787.23319. Found 787.23231.
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