| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10596241 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages |
Abstract
Semi-synthetic water-soluble analogs were synthesized from nocathiacin I through the formation of a versatile intermediate nocathiacin amine 5, and subsequent transformation via reductive amination, acylation or urea formation.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Libo Xu, Amy K. Farthing, James F. Dropinski, Peter T. Meinke, Christine McCallum, Emily Hickey, Kun Liu,