Synthesis of optically active chiral dendrimers with 1,2-diol linkages

American Chemical Society, Polymer Preprints, Division of Polymer Chemistry

Volumn 37, Issue 2, 1996, Pages 495-496

  McElhanon, James ^a   Wu, Mu Jen ^a   Escobar, Maya ^a   McGrath, Dominic V ^a  

^a UNIVERSITY OF CONNECTICUT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; DERIVATIVES; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROGEN BONDS; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL);

BENZYLOXY CARBONS; CHIRAL DENDRIMERS;

MACROMOLECULES;

EID: 0030205285     PISSN: 00323934     EISSN: None     Source Type: Conference Proceeding    
DOI: None     Document Type: Article

References (18)

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11. In an asymmetric environment: Brunner, H.; Altmann, S. Chem. Ber. 1994, 127, 2285-2296.
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13. In a symmetric environment: (a) Newkome, G.R.; Guther, R.; Moorefield, C.N.; Cardullo, F.; Echegoyen, L.; Perez-Cordero, E.; Luftmann, H. Angew. Chem. Int. Ed. Eng. 1995, 34, 2023-6. (b) Knapen, J.W.J.; van der Made, A.W.; de Wilde, J.C.; van Leeuwen, P.W.N.M.; Wijkens, P.; Grove, D.M.; van Koten, G. Nature 1994, 372, 659-63.
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15. To our knowledge, our report is only the second example of chiral dendrimer synthesis from building-blocks not derived from natural sources. See rafarance 2a.
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18. For an example of non-symmetric branching see: Percec, V.; P., C.; Unger, G.; Zhou, J. J. Am. Chem. Soc. 1995, 117, 11441.