Results 101 to 110 of about 789 (205)

Inheritance and molecular characterization of resistance to AHAS-inhibiting herbicides in rapeseed

open access: yesJournal of Integrative Agriculture, 2017
Rapeseed is a very important oil crop in China; however, its production is challenging due to the absence of effective weed management strategies. This is predominantly because of a shortage of herbicide resistance genes. Acetohydroxyacid synthase (AHAS)
Mao-long HU   +9 more
doaj   +1 more source

Iron-Catalyzed Intramolecular C–H Amination of α‑Azidyl Amides

open access: yes, 2019
Iron-catalyzed intramolecular C–H amination of aliphatic azides has recently emerged as a powerful tool for the preparation of nitrogen heterocycles. This paper reports that α-azidyl amides can be converted in high efficacy to imidazolinone compounds via
Wei Yu (43094)   +4 more
core   +1 more source

The use of mutants and transgenic plants to study amino acid metabolism.

open access: yes, 1994
Mutants of higher plants with alterations in amino acid metabolism have now been available for 20 years. Following the realization that at least four distinct classes of herbicides (phosphinothricins, glyphosates, imidazolinones and sulphonylureas) act ...
Lea, P. J., Forde, B. G.
core   +3 more sources

Efeitos de imidazolinonas e sulfoniluréias sobre a produção de sementes e emergência de plântulas de quinquilho Effects of imidazolinones and sulfonylureas on jimsonweed seed production and seedling emergence

open access: yesPlanta Daninha, 1994
Em 1990, 91 e 92 foi conduzido ensaio na Faculdade de Agronomia da UFRS, em Porto Alegre, RS, cujo objetivo foi investigar os efeitos de herbicidas aplicados durante a fase reprodutiva de quinquilho (Datura stramonium).
André Andres, Nilson G. Flecks
doaj   +1 more source

Effect of mutagenesis at serine 653 of Arabidopsis thaliana acetohydroxyacid synthase on the sensitivity to imidazolinone and sulfonylurea herbicides.

open access: yes, 1999
Resistance to sulfonylurea and imidazolinone herbicides can occur by mutations in acetohydroxyacid synthase (EC 4.1.3.18). Changing serine 653 to asparagine is known to cause insensitivity to imidazolinones but not to sulfonylureas.
Yu-Ting Lee   +5 more
core   +1 more source

Mutagenesis studies of the sensitivity of Escherichia coli acethydroxyacid synthase II to herbicides and valine

open access: yes, 2000
Acetohydroxyacid synthase (EC 4.1.3.18, also known as acetolactate synthase) isoenzyme II from Escherichia coli is inhibited by sulphonylurea and imidazolinone herbicides, although it is much less sensitive than the plant enzyme.
Lee, Y. L., Duggleby, R. G.
core   +1 more source

Un nouvel herbicide en hévéaculture - ses potentialités dans les plantations africaines

open access: yes, 1986
Un herbicide nouveau, ARSENAL, de la matière active imazapyr, de la famille des imidazolinones, est testé dans les plantations d'hévéa de Côte d'Ivoire, du Gabon et du Cameroun.
De La Serve, Michel   +2 more
core  

Imidazolinone Resistance in Oilseed Rape (Brassica napus L.): Current Status, Breeding, Molecular Markers and Prospects for Application in Hybrid Seed Purity Improvement

open access: yesHorticulturae
Resistance of agricultural crops to herbicides is an important topic that concerns many researchers. One of the most popular groups of herbicides is the imidazolinone group.
Elena Victorovna Kozar   +1 more
doaj   +1 more source

Bioassays for diagnosis of resistance to the herbicides imidazolinones in rice plants [PDF]

open access: yes, 2010
Cultivares de arroz resistentes aos herbicidas imidazolinonas têm proporcionado a utilização destes para o controle do arroz-vermelho, que é um dos principais problemas da cultura do arroz irrigado.
Delatorre, Carla Andrea   +2 more
core   +1 more source

A new synthetic route to 4-arylidene-2-phenyl-2-imidazolin-5-ones

open access: yes, 1999
378-379Condensation of aromatic aldehydes with benzoylglycine amide in saturated potassium carbonate solution yields imidazolinones 2. Eight imidazolinones have been synthesized by this method in 44- 60% yields. The reaction follows pathway (i) which
Shafi, PM, Sobha, T D
core  

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