Pentiptycene chemistry: New pentiptycene building blocks derived from pentiptycene quinones

Journal of Organic Chemistry

Volumn 71, Issue 2, 2006, Pages 844-847

  Yang, Jye Shane ^a   Ko, Ching Wei ^b  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^b NATIONAL CENTRAL UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; BROMINE; HALOGEN COMPOUNDS; NITROGEN; REACTION KINETICS; SYNTHESIS (CHEMICAL);

ALKOXY GROUP; PENTIPTYCENE CHEMISTRY; PENTIPTYCENES; QUINONES;

KETONES;

ALKANE DERIVATIVE; BROMINE DERIVATIVE; FORMALDEHYDE; HYDROXYL GROUP; IODINE DERIVATIVE; NITRILE; NITRO DERIVATIVE; PENTIPTYCENE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; DECOMPOSITION; DERIVATIZATION; REACTION ANALYSIS; SUBSTITUTION REACTION; SYNTHESIS;

EID: 30744476796     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo052158d     Document Type: Article

References (34)

1. (a) Hart, H.; Shamouilian, S.; Takehira, Y. J. Org. Chem. 1981, 46, 4427-4432.
2. (b) Hart, H.; Bashir-Hashemi, A.; Luo, J.; Meador, M. A. Tetrahedron 1986, 1641-1654.
3. For examples of conformational studies, see: (a) Yang, J.-S.; Liu, C.-P.; Lin, B.-C.; Tu, C.-W.; Lee, G.-H. J. Org. Chem. 2002, 67, 7343-7354.
4. (b) Gung, B. W.; Xue, X.; Reich, H. J. J. Org. Chem. 2005, 70, 3641-3644.
5. For examples of supramolecular structures, see: (a) Mare Veen, E.; Postma, P. M.; Jonkman, H. T.; Spek, A. L.; Feringa, B. L. Chem. Commun. 1999, 1709-1710.
6. (b) Yang, J.-S.; Liu, C.-P.; Lee, G.-H. Tetrahedron Lett. 2000, 41, 7911-7915.
7. (c) Yang, J.-S.; Lee, C.-C.; Yan, S.-L.; Chang, C.-C.; Lee, C.-C.; Leu, J.-M. J. Org. Chem. 2000, 65, 871-877.
8. (d) Zhu, X.-Z.; Chen, C.-F. J. Am. Chem. Soc. 2005, 127, 13158-13159.
9. For examples of molecular devices, see: (a) Kelly, T. R.; Bowyer, M. C.; Bhaskar, K. V.; Bebbington, D.; Garcia, A.; Lang, F.; Kim, M. H.; Jette, M. P. J. Am. Chem. Soc. 1994, 116, 3657-3658.
10. (b) Kelly, T. R.; Silva, R. A.; De Silva, H.; Jasmin, S.; Zhao, Y. J. Am. Chem. Soc. 2000, 122, 6935-6949.
11. (c) Godinez, C. E.; Zepeda, G.; Garcia-Gavibay, M. A. J. Am. Chem. Soc. 2002, 124, 4701-4707.
12. (d) Annunziata, R.; Benaglia, M.; Cinquini, M.; Raimondi, L.; Cozzi, F. J. Phys. Org. Chem. 2004, 17, 749-751.
13. For examples of chemosensory materials, see: (a) Yang, J.-S.; Swager, T. M. J. Am. Chem. Soc. 1998, 120, 5321-5322.
14. (b) Yang, J.-S.; Swager, T. M. J. Am. Chem. Soc. 1998, 120, 11864-11873.
15. (c) Yang, J.-S.; Lin, C.-S.; Hwang, C.-Y. Org. Lett. 2001, 3, 889-892.
16. For examples of light-emitting materials, see: (a) Zhu, Z.; Swager, T. M. Org. Lett. 2001, 3, 3471-3474.
17. (b) Zhao, D.; Swager, T. M. Org. Lett. 2005, 7, 4357-4360.
18. (c) Breen, C. A.; Rifai, S.; Bulvoić, V.; Swager, T. M. Nano Lett. 2005, 5, 1597-1601.
19. (a) Iiba, E.; Hirai, K.; Tomioka, H.; Yoshioka, Y. J. Am. Chem. Soc. 2002, 124, 14308-14309.
20. (b) Long, T. M.; Swager, T. M. J. Am. Chem. Soc. 2002, 124, 3826-3827.
21. (c) Long, T. M.; Swager, T. M. J. Am. Chem. Soc. 2003, 125, 14113-14119.
22. (a) Wiehe, A.; Senge, M. O.; Kurreck, H. Liebigs Ann. Recl. 1997, 1951-1963.
23. (b) Zhu, X.-Z.; Chen, C.-F. J. Org. Chem. 2005, 70, 917-924.
24. Williams, V. E.; Swager, T. M. Macromolecules 2000, 33, 4069-4073.
25. Cadogan, J. I. G.; Molina, G. A. J. Chem. Soc., Perkin Trans. 1973, 541-542.
26. (a) Beckwith, A. L. J.; Norman, R. O. C. J. Chem. Soc. B 1969 403-412.
27. (b) Hegarty, A. F. In The Chemistry of Diazonium and Diaz Groups; Patai, S., Ed.; John Wiley & Sons: New York, 1978; Part 2 Chapter 12.
28. Cadogan, J. I. G.; Roy, D. A.; Smith, D. M. J. Chem. Soc. C 1966, 1249-1250.
29. Traylor, T. G.; Hill, K. W.; Fann, W.-P.; Tsuchiya, S.; Dunlap, B. E. J. Am. Chem. Soc. 1992, 114, 1308-1312.
30. Sy, W.-W. Synth. Commun. 1992, 22, 3215-3219.
31. Mitchell, R. H.; Lai, Y.-H.; Williams, R. V. J. Org. Chem. 1979, 44, 4733-4735.
32. Hegedus, L. S. In Organometallics in Synthesis; Schlosser, M., Ed.; John Wiley & Sons: New York, 1994; Chapter 5.
33. Newman, M. S.; Boden, H. J. Org. Chem. 1961, 26, 2525-2525.
34. Raap, J.; Nieuwenhuis, S.; Creemers, A.; Hexspoor, S.; Kragl, U.; Lugtenburg, J. Eur. J. Org. Chem. 1999, 2609-2621.