@article{80e7aaa551a54c9491e4ee7896758927,
title = "Diverted total synthesis of the baulamycins and analogues reveals an alternate mechanism of action",
abstract = "The baulamycins were identified as in vitro siderophore biosynthesis inhibitors. Diverted total synthesis was used to construct the natural products and eight strategic analogues, three of which had improved inhibitory activity. Biological testing then revealed that membrane damage is the predominant mode of action in Staphylococcus aureus cells.",
author = "Steele, {Andrew D.} and Guillaume Ernouf and Lee, {Young Eun} and Wuest, {William M.}",
note = "Funding Information: This work was supported by the National Institute of General Medical Sciences (GM119426) and the National Science Foundation (CHE1755698). The NMR instruments used in this work were supported by the National Science Foundation (CHE1531620). Publisher Copyright: {\textcopyright} 2018 American Chemical Society.",
year = "2018",
month = feb,
day = "16",
doi = "10.1021/acs.orglett.8b00054",
language = "English",
volume = "20",
pages = "1126--1129",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "4",
}