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Correction
The First Stereoselective Total Synthesis of Putaminoxin E and Its Epimer and Evaluation of Their Biological Properties
Article first published online: 13 JAN 2012
DOI: 10.1002/ejoc.201101859
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Publication History
- Issue published online: 13 FEB 2012
- Article first published online: 13 JAN 2012
- Manuscript Received: 29 DEC 2011
The First Stereoselective Total Synthesis of Putaminoxin E and Its Epimer and Evaluation of Their Biological Properties†
Vol. 2012, Issue 6, 1253–1258, Article first published online: 9 DEC 2011
- Abstract
- Article
- References
- Cited By
Keywords:
- Natural products;
- Kinetic resolution;
- Metathesis;
- Enantioselectivity;
- Biological activity
A statement regarding the biological activities of the studied compounds against several bacterial organisms was incorrect. The correct wording of the paragraph beneath Table 2 on the third page of the original article1 is given below. We apologize for any confusion this may have caused.
The Authors
“Putaminoxin E (1) showed impressive activity against S. aureus and E. coli, whereas epimer 1a showed activity against P. arruginosa. Thus, it is assumed that the stereochemistry of 1 and 1a at C-9 has an important role on both the cytotoxicity and antimicrobial activity of these compounds.”
- 1C. Sudhakar, P. R. Reddy, C. G. Kumar, P. Sujitha, B. Das, Eur. J. Org. Chem. 2012, 1253–1258, preceding paper; article first published online December 9, 2011