نتایج جستجو برای: butyl ester

تعداد نتایج: 50189  

2017
Yangyang Wang Fangfang Li Xinling Ruan Jian Song Lv Lv Liyuan Chai Zhihui Yang Lin Luo

A stable bacterial consortium (LV-1) capable of degrading di-n-butyl phthalate (DBP) was enriched from river sludge. Community analysis revealed that the main families of LV-1 are Brucellaceae (62.78%) and Sinobacteraceae (14.83%), and the main genera of LV-1 are Brucella spp. (62.78%) and Sinobacter spp. (14.83%). The optimal pH and temperature for LV-1 to degrade DBP were pH 6.0 and 30°C, res...

Journal: :Langmuir : the ACS journal of surfaces and colloids 2005
F Pan P Wang K Lee A Wu N J Turro J T Koberstein

We report a simple photolithographic approach for the creation and micropatterning of chemical functionality on polymer surfaces by use of surface-active block copolymers that contain protected photoactive functional groups. The block copolymers self-assemble at the substrate-air interface to generate a surface that is initially hydrophobic with low surface tension but that can be rendered hydr...

Journal: :European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 2004
Lene Simonsen Aksel Jørgensen Eva Benfeldt Lotte Groth

The purpose was to investigate the in vivo skin penetration of four 14C-salicylic compounds using microdialysis and to relate dermal concentrations to structural features. Furthermore, to compare two in vivo retrodialysis recovery methods for estimation of true unbound extracellular concentrations. Microdialysis probes were inserted in the dermis of hairless rats. Equimolal 14C-salicylic formul...

2011
Mohd Basyaruddin Abdul Rahman Naz Chaibakhsh Mahiran Basri

Immobilized Candida antarctica lipase B, Novozym 435, was used as the biocatalyst in the esterification of adipic acid with four different isomers of butanol (n-butanol, sec-butanol, iso-butanol, and tert-butanol). Optimum conditions for the synthesis of adipate esters were obtained using response surface methodology approach with a four-factor-five-level central composite design concerning imp...

Journal: :Liquid Crystals 2022

The synthesis and characterisation of two groups nonsymmetric dimers, the 1-(4-cyanobiphenyl-4‘−yloxy)-ω-(4-butyl, 4-(1-methylpropyl) or 4-t-butylanilinebenzylidene-4’−oxy)alkanes, 1-(4-cyanobiphenyl-4‘−yl)-ω-(4-butyl, are reported. length parity flexible spacer is varied. tert-butyl homologues show higher melting points than corresponding sec-butyl n-butyl substituted suggesting that chain bra...

Journal: :International Journal of Plant and Soil Science 2023

The present study investigated the chemical constituents isolated from Azadirachta indica chloroform extract. extraction of leaves was done using Soxhlet apparatus. To isolate and identify antibacterial fraction extract, TLC-bioautography carried out. Phenol 3,5-bis (1,1-dimethyl ethyl), Phthalic acid bis (7-methyloclyl), Dido decyl phthalates, Oxalic acid, allyl hexadecyl ester, 2-Piperidinone...

Journal: :Chemistry & biology 2012
Liujie Huo Shwan Rachid Marc Stadler Silke C Wenzel Rolf Müller

Bottromycins represent a promising class of antibiotics binding to the therapeutically unexploited A-site of the bacterial ribosome. By inhibiting translation they are active against clinically important pathogens, such as vancomycin-resistant Enterococci. Structurally, bottromycins are heavily modified peptides exhibiting various unusual biosynthetic features. To set the stage for compound mod...

Journal: :The Journal of organic chemistry 2017
Ivan Zemskov Stefan Altaner Daniel R Dietrich Valentin Wittmann

Microcystins (MCs) are highly toxic natural products which are produced by cyanobacteria. They can be released to the water during harmful algal blooms and are a serious threat to animals and humans. Described is the total synthesis of the cyanotoxin microcystin-LF (MC-LF, 1a) and two derivatives thereof. Deuterated derivative 1b is of interest as an internal standard during MC quantification i...

Journal: :Molecules 2012
János Marton Brita Glaenzel Julia Roessler Daniela Golaszewski Gjermund Henriksen

The route selection and development of a convenient synthesis of 4-carboxy-4-anilidopiperidines is described. Previous routes were hampered by the low yield of the target esters as well as the inability to convert the esters to the required free acids. Considerations for large-scale production led to a modified synthesis that utilised a tert-butyl ester of 4-carboxy-4-anilidopiperidines which r...

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