Corrigendum to "Heterocyclic amines for the construction of peptoid oligomers bearing multi-dentate ligands" [Tetrahedron Lett. 49 (2008) 335] (DOI:10.1016/j.tetlet.2007.11.047);Heterocyclic amines for the construction of peptoid oligomers bearing multi-dentate ligands

Tetrahedron Letters

Volumn 49, Issue 2, 2008, Pages 335-338

  Maayan, Galia ^a   Yoo, Barney ^a   Kirshenbaum, Kent ^a  

^a NEW YORK UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2 (1,10 PHENANTHROLIN 5 YLOXY)ETHYLAMINE; 2 (2,2':6',2'' TERPYRIDIN 4' YLOXY)ETHYLAMINE; 8 HYDROXY 2 QUINOLINEMETHYLAMINE; GLYCINE; HETEROCYCLIC AMINE; HETEROCYCLIC COMPOUND; LIGAND; OLIGOMER; PEPTOID; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; SOLID PHASE SYNTHESIS;

EID: 36849010771     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.001     Document Type: Erratum

References (25)

1. Kirshenbaum K., Barron A.E., Goldsmith R.A., Armand P., Bradley E., Truong K.-T.V., Dill K.A., Cohen R.E., and Zuckermann R.N. Proc. Natl. Acad. Sci. U.S.A. 95 (1998) 4303-4308
2. Wu C.W., Sanborn T.J., Zuckermann R.N., and Barron A.E. J. Am. Chem. Soc. 123 (2001) 2958-2963
3. Wu C.W., Sanborn Huang K.T.J., Zuckermann R.N., and Barron A.E. J. Am. Chem. Soc. 123 (2001) 6778-6784
4. Fafarman A.T., Borbat P.P., Freed J.H., and Kirshenbaum K. Chem. Commun. (2007) 377-379
5. Shin S.-B.Y., Yoo B., Todaro L., and Kirshenbaum K. J. Am. Chem. Soc. 129 (2007) 3218-3225
6. Patch J.A., Kirshenbaum K., Seurynck S.L., Zuckermann R.N., and Barron A.E. Pseudo-Peptides Drug Discovery (2004) 1-31
7. Zuckermann R.N., Kerr J.M., Kent S.B.W., and Moos W.H. J. Am. Chem. Soc. 114 (1992) 10646-10647
8. Pei Y.H., and Moos W.H. Tetrahedron Lett. 35 (1994) 5825-5828
9. Horn T., Lee B.C., Dill K.A., and Zuckermann R.N. Bioconjugate Chem. 15 (2004) 428-435
10. Burkoth T.S., Fafarman A.T., Charych D.H., Connolly M.D., and Zuckermann R.N. J. Am. Chem. Soc. 125 (2003) 8841-8845
11. For example. Andres P.A., and Schubert U.S. Adv. Mater. 16 (2004) 1043-1068
12. Hofmeier H., and Schubert U.S. Chem. Soc. Rev. 33 (2004) 373-399
13. Bonnet S., Collin J.-P., Koizumi M., Mobian P., and Sauvage J.-P. Adv. Mater. 18 (2006) 1239-1250
14. Ninghai H., Katsuyuki A., and Hiroshi Y. Inorg. Chim. Acta 163 (1998) 105-113
15. Yilmaz V.T., Yilmaz F., Topcu Y., Andac O., and Guven K. J. Mol. Struct. 560 (2001) 9-13
16. Leydet Y., Bassani D.M., Jonusauskas G., and McClenaghan N.D. J. Am. Chem. Soc. 129 (2007) 8688-8689
17. La Dela M., Grisolia A., Aiello I., Crispini A., Ghedini M., Belviso S., Amati M., and Lelj F. Dalton Trans. (2004) 2424-2431
18. Wang J., Oyler K.D., and Bernhard S. Inorg. Chem. 46 (2007) 5700-5706
19. For example:. Gilmartin B.P., Ohr K., McLaughlin R.L., Koerner R., and Williams M.E. J. Am. Chem. Soc. 127 (2005) 9546-9555
20. Nicoll A.J., Miller D.J., Futterer K., Ravelli R., and Allemann R.K. J. Am. Chem. Soc. 128 (2006) 9187-9193
21. Andres P.A., Lunkwitz R., Pabst G.R., Bohn K., Wouters D., Scmatloch S., and Schubert U.S. Eur. J. Org. Chem. (2003) 3769-3776
22. +).
23. +).
24. +).
25. 4