Polyphenylene dendrimers via Diels–Alder reactions: the convergent approach
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Uwe-Martin Wiesler and Klaus Müllen
Abstract
Polyphenylene dendrimers and dendrons can be obtained using [2 + 4]cycloaddition and Knoevenagel cyclocondensation in a convergent approach.
References
G. R. Newkome,
C. N. Moorefield and
F. Vögtle,
Dendritic Molecules,
VCH,
Weinheim,
1996 Search PubMed; A. W. Bosman, H. M. Janssen and E. W. Meijer, Chem. Rev., 1999, 99, 1665 Search PubMed.
F. Morgenroth, E. Reuter and K. Müllen, Angew. Chem., 1997, 109, 647 CrossRef; Angew. Chem., Int. Ed. Engl.,
1997,
36,
631 Search PubMed; F. Morgenroth, A. J. Berresheim, M. Wagner and K. Müllen, Chem. Commun., 1998, 1139 Search PubMed.
F. Morgenroth, C. Kübel and K. Müllen, J. Mater. Chem., 1997, 7, 1207 RSC.
C. J. Hawker and J. M. J. Fréchet, Macromolecules, 1990, 23, 4726 CrossRefCAS; K. L. Wooley, C. J. Hawker and J. M. J. Fréchet, J. Chem. Soc., Perkin Trans. 1, 1991, 1059 RSC; K. L. Wooley, C. J. Hawker and J. M. J. Fréchet, J. Am. Chem. Soc., 1993, 115, 11496 CrossRefCAS.
S. Takahashi, Y. Kuroyama, K. Sonogashira and N. Hagihara, Synthesis, 1980, 627 CrossRefCAS.
F. Morgenroth and K. Müllen, Tetrahedron, 1997, 53, 15 349 CrossRefCAS.
CERIUS2, Molecular Simulations Inc., Waltham, MA, USA. For more
details see ref. 3. Additional data are to be published.
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