نتایج جستجو برای: trifluoromethyl

تعداد نتایج: 2599  

Journal: :Inorganic chemistry 2002
Yuichi Terazono Brian O Patrick David H Dolphin

Zinc(II) complexes of antipodal beta-tetrasubstituted meso-tetraphenylporphyrin with trifluoromethyl (Zn(TPP(CF(3))(4)) (1a)), bromine (Zn(TPPBr(4)) (2a)), and methyl groups (Zn(TPP(CH(3))(4)) (3a)) were synthesized in order to examine the steric and the electronic effects of trifluoromethyl groups on the macrocycle. The analysis of X-ray crystal structures of the five-coordinate complexes Zn(T...

Journal: :Journal of AOAC International 2001
T D Hubert C Vue J A Bernardy D L Van Horsen M I Rossulek

3-Trifluoromethyl-4-nitrophenol (TFM) is a pesticide used for the selective control of sea lampreys (Petromyzon marinus) in stream and river tributaries of the Great Lakes. To determine concentrations of TFM and TFM glucuronide in the edible fillet tissue of fish during sea lamprey control treatments, an analytical method was developed to determine the concentrations of these residues in rainbo...

Journal: :The Biochemical journal 1991
J M Camadro M Matringe R Scalla P Labbe

Diphenyl ethers (DPEs) and related herbicides are powerful inhibitors of protoporphyrinogen oxidase, an enzyme involved in the biosynthesis of haems and chlorophylls. The inhibition kinetics of protoporphyrinogen oxidase of various origins by four DPEs, (methyl)-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid (acifluorfen and its methyl ester, acifluorfen-methyl), methyl-5-[2-chloro...

Journal: :Plant physiology 1985
M P Ensminger F D Hess

Photosynthesis is not required for the toxicity of diphenyl ether herbicides, nor are chloroplast thylakoids the primary site of diphenyl ether herbicide activity. Isolated spinach (Spinacia oleracea L.) chloroplast fragments produced malonyl dialdehyde, indicating lipid peroxidation, when paraquat (1,1'-dimethyl-4,4'-bipyridinium ion) or diuron [3-(3,4-dichlorophenyl)-1,1-dimethylurea] were ad...

2018
Guan-bao Li Chao Zhang Chun Song Yu-dao Ma

The introduction of trifluoromethyl groups into organic molecules has attracted great attention in the past five years. In this review, we describe the recent efforts in the development of trifluoromethylation via copper catalysis using nucleophilic, electrophilic or radical trifluoromethylation reagents.

Journal: :Bioorganic & medicinal chemistry letters 2006
Jie-Fei Cheng Chi Ching Mak Yujin Huang Richard Penuliar Masahiro Nishimoto Lin Zhang Mi Chen David Wallace Thomas Arrhenius Donald Chu Guang Yang Miguel Barbosa Rick Barr Jason R B Dyck Gary D Lopaschuk Alex M Nadzan

A series of heteroaryl-substituted bis-trifluoromethyl carbinols were prepared and evaluated as malonyl-CoA decarboxylase (MCD) inhibitors. Some thiazole-based derivatives showed potent in vitro MCD inhibitory activities and significantly increased glucose oxidation rates in isolated working rat hearts.

Journal: :Bioscience, biotechnology, and biochemistry 2009
Ryo Murashige Yuta Murai Yasumaru Hatanaka Makoto Hashimoto

The Friedel-Crafts reaction with 3-(3-methoxyphenyl)-3-(trifluoromethyl)-3H-diazirine and optically active N-TFA-Asp(Cl)-OMe in triflic acid afforded homophenylalanine derivatives without any loss of the optical purity.

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