Front Cover: SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs (Chem. Eur. J. 66/2020)
The design and total synthesis of dramatically simplified leupylogs is presented. They demonstrate similar highly potent antifungal activities as the natural leupyrrins, as depicted by a balanced IC50 weighing scale. The origin of the secondary metabolites from the myxobacterium Sorangium cellulosum...
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Veröffentlicht in: | Chemistry : a European journal 2020-11, Vol.26 (66), p.15047-15047 |
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container_issue | 66 |
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container_title | Chemistry : a European journal |
container_volume | 26 |
creator | Wosniok, Paul R. Knopf, Christopher Dreisigacker, Sandra Orozco‐Rodriguez, J. Manuel Hinkelmann, Bettina Mueller, Peter P. Brönstrup, Mark Menche, Dirk |
description | The design and total synthesis of dramatically simplified leupylogs is presented. They demonstrate similar highly potent antifungal activities as the natural leupyrrins, as depicted by a balanced IC50 weighing scale. The origin of the secondary metabolites from the myxobacterium Sorangium cellulosum is illustrated by its fruiting bodies while the flask portrays the synthetic endeavors which have led to the discovery of leupylogs. More information can be found in the Communication by D. Menche et al. on page 15074. |
doi_str_mv | 10.1002/chem.202003844 |
format | Article |
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subjects | antifungal agents Leupylogs natural products SAR studies total synthesis |
title | Front Cover: SAR Studies of the Leupyrrins: Design and Total Synthesis of Highly Potent Simplified Leupylogs (Chem. Eur. J. 66/2020) |
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