BOP-mediated one-pot synthesis of C5-symmetric macrocyclic pyridone pentamers

Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1cc14377h

Title:	BOP-mediated one-pot synthesis of C5-symmetric macrocyclic pyridone pentamers
Authors:	Du, Z. Ren, C. Ye, R. Shen, J. Maurizot, V. Lu, Y. Wang, J. Zeng, H.
Issue Date:	14-Dec-2011
Citation:	Du, Z., Ren, C., Ye, R., Shen, J., Maurizot, V., Lu, Y., Wang, J., Zeng, H. (2011-12-14). BOP-mediated one-pot synthesis of C5-symmetric macrocyclic pyridone pentamers. Chemical Communications 47 (46) : 12488-12490. ScholarBank@NUS Repository. https://doi.org/10.1039/c1cc14377h
Abstract:	We report here, for the first time, the BOP-mediated one-pot macrocyclization that is facilitated and guided by internally placed intramolecular H-bonds to allow for the highly selective formation of five-residue cation-binding macrocycles. © 2011 The Royal Society of Chemistry.
Source Title:	Chemical Communications
URI:	http://scholarbank.nus.edu.sg/handle/10635/93211
ISSN:	13597345
DOI:	10.1039/c1cc14377h
Appears in Collections:	Staff Publications

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