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Correction: Triamide macrocyclic chloride receptors via a one-pot tandem reduction–condensation–cyclization reaction
Harekrushna
Behera
a,
Venkatachalam
Ramkumar
a and
Nandita
Madhavan
*ab
aDepartment of Chemistry, Indian Institute of Technology, Madras, Chennai, Tamil Nadu 600036, India. E-mail: nanditam@chem.iitb.ac.in
bDepartment of Chemistry, Indian Institute of Technology, Bombay, Mumbai, Maharashtra 400076, India
First published on 31st May 2017
Abstract
Correction for ‘Triamide macrocyclic chloride receptors via a one-pot tandem reduction–condensation–cyclization reaction’ by Harekrushna Behera, et al., Org. Biomol. Chem., 2017, DOI: 10.1039/c7ob00642j.
The authors regret that some highly relevant citations reporting the synthesis of furan based triamide macrocycles were missed.
Therefore the sentence “To the best of our knowledge the only one-pot method for obtaining triamides (with a Cn symmetry) from the corresponding monomer was reported by Kilbinger and co-workers.42” should be replaced by “Pyridyl based triamide macrocycles have been synthesized without the use of coupling reagents by Kilbinger and co-workers, while Chakraborty and co-workers have developed a variety of elegant furan based chiral as well as achiral triamide macrocycles using coupling reagents.42”
The corrected reference 42 is shown below:
42 (a) C. Storz, M. Badoux, C. M. Hauke, T. S. Šolomek, A. Kühnle, T. Bally and A. F. Kilbinger, J. Am. Chem. Soc., 2014, 136, 12832–12835; (b) T. K. Chakraborty, S. Tapadar and S. K. Kumar, Tetrahedron Lett., 2002, 43, 1317–1320; (c) T. K. Chakraborty, S. Tapadar, T. V. Raju, J. Annapurna and H. Singh, Synlett, 2004, 2484–2488; (d) T. K. Chakraborty, E. Bikshapathy, R. Nagaraj, M. Vairamani, S. Kiran Kumar, and A. C. Kunwar, J. Org. Chem., 2003, 68, 6257–6263.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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