Results 181 to 190 of about 8,235 (246)

Structure of a norbornane‐fused pentacyclic isoxazoline [PDF]

open access: possibleMagnetic Resonance in Chemistry, 1990
AbstractThe steric structure of a pentacyclic adduct formed as a by‐product in a retro‐Diels‐Alder reaction was elucidated by 1H and 13C NMR spectroscopy, making use of double resonance and differential nuclear Overhauser effect measurements.
Sohár Pál   +4 more
openaire   +1 more source

Synthesis, spectroscopic characterization (FT-IR, NMR) and DFT computational studies of new isoxazoline derived from acridone

, 2021
In this study, a new isoxazoline derived from acridone, 10‐{[3‐(4‐chlorophenyl)‐4,5‐dihydro‐1,2‐oxazol‐5 yl]methyl} acridone (3) was successfully synthesized and characterized by FT-IR, 1H NMR, 13C NMR and HRMS.
Mohammed Aarjane   +3 more
semanticscholar   +1 more source

Strong deshielding in aromatic isoxazolines

Magnetic Resonance in Chemistry, 2015
AbstractVery strong proton deshielding was found in di/tri‐aromatic isoxazoline regioisomers prepared from acridin‐4‐yl dipolarophiles and stable benzonitrile oxides (BNO). Three alkenes, (acridin‐4‐yl)‐CHCH‐R (R = COOCH3, Ph, and CONH2), reacted with three BNO dipoles (2,4,6‐trimethoxy, 2,4,6‐trimethyl, 2,6‐dichloro) to give pairs of target ...
Lucia, Ungvarská Maľučká   +3 more
openaire   +2 more sources

Construction of Cholesterol Oxime Ether Derivatives Containing Isoxazoline/Isoxazole Fragments and Their Agricultural Bioactive Properties/Control Efficiency.

Journal of Agricultural and Food Chemistry, 2021
To explore natural-product-based pesticidal candidates and high value-added application of cholesterol in agriculture, oximinoether derivatives of cholesterol-containing isoxazoline/isoxazole fragments (I-1∼I-16 and II-1∼II-18) were semiprepared by ...
Hui Xu, Kong-Yan Zhang, M. Lv, Meng Hao
semanticscholar   +1 more source

Rational Design and Synthesis of Isoxazoline Derivatives with Low Bee-Toxicity Based on Bee GABA Receptors.

Journal of Agricultural and Food Chemistry
The isoxazoline insecticide, such as fluralaner, exhibits strong insecticidal activity against pests while showing no cross-resistance. However, due to its toxicity to bees, the use of Fluralaner is restricted in veterinary antiparasitic applications ...
Jianrong Yang   +6 more
semanticscholar   +1 more source

Solid-Phase Synthesis of Isoxazolines

Journal of Combinatorial Chemistry, 2002
The polymer-supported synthesis of isoxazolines is described via nitrile oxide intermediates, starting from primary nitroalkanes in a one-pot process.
S, Chandrasekhar   +3 more
openaire   +2 more sources

Isoxazoline

2005
The first part of the presented work deals with the enantioselective synthesis of isoxazolines. The synthetic approach involves the asymmetrically catalysed 1,3-dipolar cycloaddition of nitrones to acetylenes. Therefore electrondeficient mono- and bifunctionalysed as well as electronrich triplebond systems, in combination with electronrich and ...
openaire   +3 more sources

New Isoxazoline Cyclopropyl-Picolinamide Derivatives as Potential Insecticides.

Journal of Agricultural and Food Chemistry
Isoxazoline insecticides exhibit broad-spectrum insecticidal activity against insect pests. However, the high toxicity to honeybees limits their application in pest management. To explore reducing the toxicity of isoxazoline derivatives to bees, a series
Xiangmin Song   +7 more
semanticscholar   +1 more source

Discovery of new N-Phenylamide Isoxazoline derivatives with high insecticidal activity and reduced honeybee toxicity.

Pesticide Biochemistry and Physiology
Isoxazoline is a novel structure with strong potential for controlling agricultural insect pests, but its high toxicity to honeybees limits its development in agriculture.
Yongchao Gao   +5 more
semanticscholar   +1 more source

Structure of a substituted isoxazoline

Acta Crystallographica Section C Crystal Structure Communications, 1987
L'oxyde de cyano-3 tetramethyl-4,4,5,5 dihydro-4,5 isoxazole, C 8 H 12 N 2 O 2 , cristallise dans le systeme orthorhombique, groupe Pna2 1 et sa structure est affinee jusqu'a R=0,065.
C. George, R. Gilardi
openaire   +1 more source

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