286942-91-4Relevant academic research and scientific papers
Synthesis and structural analysis of the active enantiomer of famoxadone, a potent inhibitor of cytochrome bc1
Zheng, Ya-Jun,Shapiro, Rafael,Marshall, William J.,Jordan, Douglas B.
, p. 1059 - 1062 (2000)
Famoxadone is a newly commercialized fungicide and potent Q(O)-site inhibitor of cytochrome bc1. The S-(-)-enantiomer of famoxadone (the active component) was synthesized by two routes and was analyzed computationally and by X-ray crystallography. The molecule displays an extended conformation with flexibility in the structure imparted by the two terminal phenyl groups. In the crystal lattice, intermolecular hydrogen bonds occur between the NH and the oxygen atoms of the heterocycle. (C) 2000 Elsevier Science Ltd. All rights reserved.
Famoxadone: The discovery and optimisation of a new agricultural fungicide
Sternberg, Jeffrey A.,Geffken, Detlef,Adams Jr., John B.,Poestages, Reiner,Sternberg, Charlene G.,Campbell, Carlton L.,Moberg, William K.
, p. 143 - 152 (2007/10/03)
Famoxadone (3-anilino-5-methyl-5-(4-phenoxyphenyl)-1,3-oxazolidine-2,4-dione), is a new agricultural fungicide recently commercialized by DuPont under the trade name Famoxate. Famoxadone is a member of a new class of oxazolidinone fungicides th
