نتایج جستجو برای: benzoates

تعداد نتایج: 2205  

Journal: :Organic chemistry frontiers : an international journal of organic chemistry 2015
Jennifer M Crawford Kyle E Shelton Emily K Reeves Bryce K Sadarananda Dipannita Kalyani

This manuscript describes a Ni-catalyzed method for the direct arylation of azoles using benzoates. Perfluorophenyl and 2-nitrobenzoates participate in these reactions to afford the corresponding products in modest to good yields. The efficiency of the arylations with perfluorobenzoates is highly dependent on both the degree and position of fluorine atoms in the benzoates.

Journal: :Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 2003
Midori Yasuda Tamiyoshi Sonda Tomoko Hiraoka Aki Horita Masaaki Tabata

The retention behavior and mechanism of methyl, ethyl, propyl, isopropyl, buthyl and isobuthyl benzoates have been studied at different eluent compositions of aqueous mixtures with water-soluble organic solvents (methanol, ethanol, 1-propanol, 2-propanol, acetonitrile (AN), 1,4-dioxane and tetrahydrofuran (THF)) in RPLC. The retention of the solutes is discussed based on the solvent composition...

2015
Maja Miškulin Nika Pavlović Aida Mujkić Jelena Vlahović

1University of Osijek, Faculty of Medicine, Josipa Huttlera 4, 31 000 Osijek, Croatia 2Institute of Public Health for the Osijek-Baranja County, Franje Krežme 1, 31 000 Osijek, Croatia 3University of Zagreb, School of Medicine, Andrija Štampar School of Public Health, Rockefellerova 4, 10000 Zagreb, Croatia Original scientific paper Summary Introduction: Attention deficit hyperactivity disorder...

Journal: :The Journal of organic chemistry 2013
Takeo Nakano Takahiro Soeta Kohei Endo Katsuhiko Inomata Yutaka Ukaji

The sequential 1,4-elimination reaction of (E)-4-alkoxy-2-butenyl benzoates and [1,2]-Wittig rearrangement gave (2Z,4E)-2,4-pentadien-1-ols stereoselectively. Z-Selective formation of intermediary vinyl ethers, whose stereochemistry was well elucidated by the "syn-effect", was achieved by treatment of the 2-butenyl benzoates with KOH in the presence of Pd catalyst. The subsequent [1,2]-Wittg re...

2015
Karina Mroczyńska Małgorzata Kaczorowska Erkki Kolehmainen Ireneusz Grubecki Marek Pietrzak Borys Ośmiałowski

The association of substituted benzoates and naphthyridine dianions was used to study the complexation of dibutyltriuret. The title molecule is the simplest molecule able to form two intramolecular hydrogen bonds. The naphthyridine salt was used to break two intramolecular hydrogen bonds at a time while with the use of substituted benzoates the systematic approach to study association was achie...

Journal: :Catalysts 2023

The catalytic activity and cyclic catalysis of different methyl benzoates were studied by using a series Lewis solid acid catalysts. iron-supported zirconium/titanium catalysts characterized FTIR, SEM, XRD, BET. details verified that the catalyst catalyzed reactions 31 benzoic acids with substituents methanol. In addition, mechanism was revealed according to microstructure, strength, specific s...

Journal: :Applied and environmental microbiology 1998
U Rode R Müller

Iodinated X-ray contrast agents are considered to be nondegradable by microorganisms. The decomposition of the ionic X-ray contrast agents Diatrizoate (3,5-di(acetamido)-2,4,6-triiodobenzoic acid) and Iodipamide (3,3'-adipoyl-diimino-di(2,4,6-triiodobenzoic acid) and related triiodinated benzoates (Acetrizoate [3-acetylamino-2,4, 6-triiodobenzoic acid] and Aminotrizoate [3-amino-2,4, 6-triiodob...

Journal: :Applied and environmental microbiology 1991
A Contreras S Molin J L Ramos

A model conditional-suicide system to control genetically engineered microorganisms able to degrade substituted benzoates is reported. The system is based on two elements. One element consists of a fusion between the promoter of the Pseudomonas putida TOL plasmid-encoded meta-cleavage pathway operon (P(m)) and the lacI gene encoding Lac repressor plus xylS, coding for the positive regulator of ...

Journal: :Biochemistry 2001
S J Admiraal C T Walsh C Khosla

The rifamycin synthetase is primed with a 3-amino-5-hydroxybenzoate starter unit by a loading module that contains domains homologous to the adenylation and thiolation domains of nonribosomal peptide synthetases. Adenylation and thiolation activities of the loading module were reconstituted in vitro and shown to be independent of coenzyme A, countering literature proposals that the loading modu...

Journal: :Bulletin of the Chemical Society of Japan 1969

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