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Inter alia: a) Conjugated Polymers and Related Materials: The Interconnection of Chemical and Electronic Structure (Eds.: W. R. Salaneck, I. Lundström, B. Ranby), Oxford University Press: Oxford, 1993; b) Photonic and Optoelectronic Polymers (Eds.: S. A. Jenekhe, K. J. Wynne), American Chemical Society: Washington D. C., 1995; c) Nonlinear Optics of Organic Molecules and Polymers (Eds.: H. S. Nalwa, S. Miyata), CRC Press: Boca Raton, FL, 1997;
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Inter alia: a) Conjugated Polymers and Related Materials: The Interconnection of Chemical and Electronic Structure (Eds.: W. R. Salaneck, I. Lundström, B. Ranby), Oxford University Press: Oxford, 1993; b) Photonic and Optoelectronic Polymers (Eds.: S. A. Jenekhe, K. J. Wynne), American Chemical Society: Washington D. C., 1995; c) Nonlinear Optics of Organic Molecules and Polymers (Eds.: H. S. Nalwa, S. Miyata), CRC Press: Boca Raton, FL, 1997;
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Inter alia: a) Conjugated Polymers and Related Materials: The Interconnection of Chemical and Electronic Structure (Eds.: W. R. Salaneck, I. Lundström, B. Ranby), Oxford University Press: Oxford, 1993; b) Photonic and Optoelectronic Polymers (Eds.: S. A. Jenekhe, K. J. Wynne), American Chemical Society: Washington D. C., 1995; c) Nonlinear Optics of Organic Molecules and Polymers (Eds.: H. S. Nalwa, S. Miyata), CRC Press: Boca Raton, FL, 1997;
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Inter alia: a) R. Hoffmann, T. Hughbanks, M. Kertesz, P. H. Bird, J. Am. Chem. Soc. 1983, 105, 4831-4832; b) R. L. Johnston, R. Hoffmann, J. Am. Chem. Soc. 1989, 111, 810-819; c) A. T. Balaban, Comput. Math. Appl. 1989, 17, 397-416; d) R. H. Baughman, D. S. Galvão, Nature 1993, 365, 735-737; e) S. A. Best, P. A. Bianconi, K. M. Merz, Jr., J. Am. Chem. Soc. 1995, 117, 9251-9258; f) D. J. Klein, H. Zhu in From Chemical Topology to Three-Dimensional Geometry (Ed: A. T. Balaban), Plenum, New York, 1997, pp. 297-341; g) A. T. Balaban in Theoretical Organic Chemistry (Ed.: C. Párkányi), Elsevier, Amsterdam, 1998, pp. 381-403.
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Inter alia: a) R. Hoffmann, T. Hughbanks, M. Kertesz, P. H. Bird, J. Am. Chem. Soc. 1983, 105, 4831-4832; b) R. L. Johnston, R. Hoffmann, J. Am. Chem. Soc. 1989, 111, 810-819; c) A. T. Balaban, Comput. Math. Appl. 1989, 17, 397-416; d) R. H. Baughman, D. S. Galvão, Nature 1993, 365, 735-737; e) S. A. Best, P. A. Bianconi, K. M. Merz, Jr., J. Am. Chem. Soc. 1995, 117, 9251-9258; f) D. J. Klein, H. Zhu in From Chemical Topology to Three-Dimensional Geometry (Ed: A. T. Balaban), Plenum, New York, 1997, pp. 297-341; g) A. T. Balaban in Theoretical Organic Chemistry (Ed.: C. Párkányi), Elsevier, Amsterdam, 1998, pp. 381-403.
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[7] The 27% increase in step a reflects our refinement of the in situ protiodesilylation/alkynlation protocol. The decrease of about 10% in the macrocyclization step reflects better purification of the final product.
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44
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85037482493
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note
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13C NMR signals in the alkyl region.
-
-
-
|