A convenient route to diversely substituted icosahedral closomer nanoscaffolds

Journal of the American Chemical Society

Volumn 133, Issue 32, 2011, Pages 12382-12385

  Jalisatgi, Satish S ^a   Kulkarni, Vikas S ^a   Tang, Betty ^a   Houston, Zachary H ^a   Lee, Mark W ^a   Hawthorne, M Frederick ^a  

^a UNIVERSITY OF MISSOURI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANCHORING GROUPS; BIOMEDICAL APPLICATIONS; CHLOROFORMATES; MONODISPERSE; NANOSCAFFOLDS; POLYHEDRAL BORANES; PRIMARY AMINES; SHORT REACTION TIME;

MEDICAL APPLICATIONS;

SYNTHESIS (CHEMICAL);

AMINE; CARBAMIC ACID; CARBAMIC ACID DERIVATIVE; CARBONIC ACID; CHLOROFORM; DODECACARBAMATE; HYDROXYL GROUP; MOLECULAR SCAFFOLD; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL STRUCTURE; PH; PURIFICATION; ROOM TEMPERATURE; SUBSTITUTION REACTION; SYNTHESIS;

BORANES; CARBAMATES; CARBONATES; DRUG CARRIERS; MODELS, MOLECULAR; NANOSTRUCTURES;

EID: 80051583888     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja204488p     Document Type: Article

References (25)

1. Molema, G. Drug Targeting: Organ-Specific Strategies; Wiley-VCH, Inc.: New York, NY, 2001; Vol. 12.
2. Peer, D.; Karp, J. M.; Hong, S.; Farokhzad, O. C.; Margalit, R.; Langer, R. Nat. Nanotechnol. 2007, 2, 751-760
3. Torchilin, V. P. Adv. Drug. Delivery Rev. 2006, 58, 1532-1555
4. Bayer, M. J.; Hawthorne, M. F. Inorg. Chem. 2004, 43, 2018-2020
5. Peymann, T.; Knobler, C. B.; Khan, S. I.; Hawthorne, M. F. Angew. Chem., Int. Ed. 2001, 40, 1664-1667
6. Maderna, A.; Knobler, C. B.; Hawthorne, M. F. Angew. Chem., Int. Ed. 2001, 40, 1662-1664
7. Li, T.; Jalisatgi, S. S.; Bayer, M. J.; Maderna, A.; Khan, S. I.; Hawthorne, M. F. J. Am. Chem. Soc. 2005, 127, 17832-17841
8. Farha, O. K.; Julius, R. L.; Lee, M. W.; Huertas, R. E.; Knobler, C. B.; Hawthorne, M. F. J. Am. Chem. Soc. 2005, 127, 18243-18251
9. Lee, M. W.; Farha, O. K.; Hawthorne, M. F.; Hansch, C. H. Angew. Chem., Int. Ed. 2007, 46, 3018-3022
10. Goswami, L. N.; Chakravarty, S.; Lee, M. W.; Jalisatgi, S. S.; Hawthorne, M. F. Angew. Chem., Int. Ed. 2011, 50, 4689-4691
11. Green, T. W.; Wuts, P. G. M. Greene's Protective Groups in Organic Synthesis, 3 rd ed.; John Wiley & Sons, Inc.: New York, 1999.
12. Taylor, M. J. J. Chem. Eng. Data 1978, 23, 308-313
13. Espinosa, S.; Bosch, E.; Rosés, M. Anal. Chim. Acta 2002, 454, 157-166
14. Travers, F.; Douzou, P. Biochimie 1974, 56, 509-514
15. Aguilar-Moncayo, M.; Garcia-Moreno, M. I.; Stuetz, A. E.; Garcia Fernandez, J. M.; Wrodnigg, T. M.; Mellet, C. O. Bioorg. Med. Chem. 2010, 18, 7439-7445
16. Prodi, L. B., F.; Montalti, M.; Zaccheroni, N. Chem.-Eur. J. 1999, 5, 445
17. Prodi, L.; Montalti, M.; Zaccheroni, N.; Dallavalle, F.; Folesani, G.; Lanfranchi, M.; Corradini, R.; Pagliari, S.; Marchelli, R. Helv. Chim. Acta 2001, 84, 690-706
18. Chen, Q.-Y.; Chen, C.-F. Tetrahedron Lett. 2004, 46, 165-168
19. Faust, A.; Waschkau, B.; Waldeck, J.; Höltke, C.; Breyholz, H.-J.; Wagner, S.; Kopka, K.; Heindel, W.; Schäfers, M.; Bremer, C. Bioconjugate Chem. 2008, 19, 1001-1008
20. Thomas, J. R.; Liu, X.; Hergenrother, P. J. J. Am. Chem. Soc. 2005, 127, 12434-12435
21. Vögtle, F.; Gestermann, S.; Kauffmann, C.; Ceroni, P.; Vicinelli, V.; De Cola, L.; Balzani, V. J. Am. Chem. Soc. 1999, 121, 12161-12166
22. Paranjpe, P. V.; Stein, S.; Sinko, P. J. Anti-Cancer Drugs 2005, 16, 763-775
23. Abu Ajaj, K.; Graeser, R.; Fichtner, I.; Kratz, F. Cancer Chemother. Pharmacol. 2009, 64, 413-418
24. Vasiljeva, O.; Papazoglou, A.; Krueger, A.; Brodoefel, H.; Korovin, M.; Deussing, J.; Augustin, N.; Nielsen, B. S.; Almholt, K.; Bogyo, M.; Peters, C.; Reinheckel, T. Cancer Res. 2006, 66, 5242-5250
25. Obermajer, N.; Kocbek, P.; Repnik, U.; Kuznik, A.; Cegnar, M.; Kristi, J.; Kos, J. FEBS J. 2007, 274, 4416-4427