Results 151 to 160 of about 3,055 (208)
Efficacy of an oral combination of afoxolaner and milbemycin oxime for the prevention of transmission of Babesia canis by Dermacentor reticulatus ticks to dogs. [PDF]
Parasit VectorsTielemans E +3 more
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Adaptive alcohols-alcohols cross-coupling via TFA catalysis: access of unsymmetrical ethers. [PDF]
BMC ChemLiu C, Liang J, Liang Y, Ouyang L, Li Y.
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Electrocatalytic Isoxazoline–Nanocarbon Metal Complexes
Journal of the American Chemical Society, 2021We report the synthesis of new carbon-nanomaterial-based metal chelates that enable effective electronic coupling to electrocatalytic transition metals. In particular, multiwalled carbon nanotubes (MWCNTs) and few-layered graphene (FLG) were covalently functionalized by a microwave-assisted cycloaddition with nitrile oxides to form metal-binding ...
Shao-Xiong Lennon Luo +3 more
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Journal of the Chemical Society C: Organic, 1971
The reaction paths leading from ethyl propiolate to isoxazolin-5-one (II) and isoxazolin-3-one (III) are discussed and shown to be pH-dependent. The chemical and tautomeric properties of compound (II) are consistent with the known behaviour of its derivatives.
DE SARLO, FRANCESCO +2 more
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The reaction paths leading from ethyl propiolate to isoxazolin-5-one (II) and isoxazolin-3-one (III) are discussed and shown to be pH-dependent. The chemical and tautomeric properties of compound (II) are consistent with the known behaviour of its derivatives.
DE SARLO, FRANCESCO +2 more
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Insecticidal quinoline and isoquinoline isoxazolines
Bioorganic & Medicinal Chemistry Letters, 2014A series of quinoline and isoquinoline isoxazolines have been designed as pesticides for crop protection. Herein we reported the chemical synthesis, biological activity and structure-activity relationships. The isoquinoline derivative, such as 3i, is discovered as potent new class of isoxazoline insecticide which is competitive with commercial ...
Ming, Xu +5 more
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Strong deshielding in aromatic isoxazolines
Magnetic Resonance in Chemistry, 2015AbstractVery 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)‐CHCH‐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
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