| Literature DB >> 26321602 |
Jeffrey B Epp1, Anita L Alexander2, Terry W Balko2, Ann M Buysse2, William K Brewster2, Kristy Bryan2, John F Daeuble2, Stephen C Fields2, Roger E Gast2, Renard A Green2, Nicholas M Irvine2, William C Lo2, Christian T Lowe2, James M Renga2, John S Richburg2, James M Ruiz2, Norbert M Satchivi2, Paul R Schmitzer2, Thomas L Siddall2, Jeffery D Webster2, Monte R Weimer2, Gregory T Whiteker2, Carla N Yerkes2.
Abstract
Multiple classes of commercially important auxin herbicides have been discovered since the 1940s including the aryloxyacetates (2,4-D, MCPA, dichlorprop, mecoprop, triclopyr, and fluroxypyr), the benzoates (dicamba), the quinoline-2-carboxylates (quinclorac and quinmerac), the pyrimidine-4-carboxylates (aminocyclopyrachlor), and the pyridine-2-carboxylates (picloram, clopyralid, and aminopyralid). In the last 10 years, two novel pyridine-2-carboxylate (or picolinate) herbicides were discovered at Dow AgroSciences. This paper will describe the structure activity relationship study that led to the discovery of the 6-aryl-picolinate herbicides Arylex™ active (2005) and Rinskor™ active (2010). While Arylex was developed primarily for use in cereal crops and Rinskor is still in development primarily for use in rice crops, both herbicides will also be utilized in additional crops.Entities:
Keywords: 6-Aryl-picolinate; Arylex; Halauxifen; Halauxifen-methyl; Picolinate; Rinskor
Mesh：
Substances：
Year: 2015 PMID： 26321602 DOI： 10.1016/j.bmc.2015.08.011
Source DB: PubMed Journal: Bioorg Med Chem ISSN： 0968-0896 Impact factor: 3.641