Supporting Information
| Supporting Information File 1: This file describes the full experimental details and characterization data of compounds 1–3, 4a–f, 6a and 7a. | ||
| Format: DOC | Size: 72.0 KB | Download |
| Supporting Information File 2: 1H NMR spectra of compounds 4a–d. | ||
| Format: DOC | Size: 7.1 MB | Download |
| Supporting Information File 3: 13C NMR spectra of compounds 4a–b and 4d–e. | ||
| Format: DOC | Size: 8.9 MB | Download |
Cite the Following Article
New acylides: synthesis of 3-O-[γ-(4-oxo-2-aryl-thiazolidin-3-yl)butyryl]erythromycin A derivatives
Deepa Pandey, Wahajul Haq and Seturam B. Katti
Beilstein J. Org. Chem. 2008, 4, No. 14.
https://doi.org/10.3762/bjoc.4.14
How to Cite
Pandey, D.; Haq, W.; Katti, S. B. Beilstein J. Org. Chem. 2008, 4, No. 14. doi:10.3762/bjoc.4.14
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- Liang, J.-H.; Han, X. Structure-activity relationships and mechanism of action of macrolides derived from erythromycin as antibacterial agents. Current topics in medicinal chemistry 2013, 13, 3131–3164. doi:10.2174/15680266113136660223
- Cameron, E. J.; McSharry, C.; Chaudhuri, R.; Farrow, S. N.; Thomson, N. C. Long‐term macrolide treatment of chronic inflammatory airway diseases: risks, benefits and future developments. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2012, 42, 1302–1312. doi:10.1111/j.1365-2222.2012.03979.x
