نتایج جستجو برای: oxalyl

تعداد نتایج: 230  

2002
J. R. Babu A. E. Brink

A method has been developed for the synthesis of semicrystalline poly(arylene ether ether sulfide) materials by first preparing a soluble, amorphous sulfoxide containing precursor, then rapidly reducing the sulfoxide moiety to sulfide. The sulfoxide polymers are synthesized using conventional nucleophilic aromatic substitution reactions between difluorodiphenyl sulfoxide and diphenols. Reductio...

Journal: :Analytical biochemistry 1980
J E Bishop A K Hajra

A simple and reliable method, based on that described by W. Seubert (1960, Biochem Prep. 7, 80-83), has been developed for the chemical synthesis of radioactive acyl coenzyme A’s. I-14C-labeled fatty acids (palmitic, oleic, and linoleic) are converted to their acyl chlorides with oxalyl chloride. The [l-14C]acyl chlorides are then condensed with a twoto three-fold molar excess of coenzyme A in ...

Journal: :iranian journal of science and technology (sciences) 2014
a. jarrahpour

thionyl chloride (or oxalyl chloride) has been used as an efficient and cheap acid activator for one-pot synthesis of β-lactams in good to excellent yields by reaction between imines and acids in the presence of triethylamine at room temperature.

Journal: :Chemistry 2013
Niall P Kenny Kamalraj V Rajendran Elizabeth V Jennings Declan G Gilheany

In contrast to tertiary phosphine oxides, the deoxygenation of aminophosphine oxides is effectively impossible due to the need to break the immensely strong and inert PO bond in the presence of a relatively weak and more reactive PN bond. This long-standing problem in organophosphorus synthesis is solved by use of oxalyl chloride, which chemoselectively cleaves the PO bond forming a chloroph...

Journal: :Nucleic acids research 1994
N N Polushin J S Cohen

Oligonucleotides bearing a terminal lipophilic group attached through a biodegradable ester bond should be useful as antisense pro-drugs with improved cellular uptake. The synthesis of 5'-ester oligonucleotides is, however, problematic due to lability of the ester bond during aqueous ammonia treatment that is commonly used for the deprotection of synthetic oligonucleotides. The synthesis of 5'-...

2010
Janja Makarević Milan Jokić Leo Frkanec Vesna Čaplar Nataša Šijaković Vujičić Mladen Žinić

In this work we report on gelation properties, self-assembly motifs, chirality effects and morphological characteristics of gels formed by chiral retro-dipeptidic gelators in the form of terminal diacids (1a-5a) and their dimethyl ester (1b-5b) and dicarboxamide (1c-5c) derivatives. Terminal free acid retro-dipeptides (S,S)-bis(LeuLeu) 1a, (S,S)-bis(PhgPhg) 3a and (S,S)-bis(PhePhe) 5a showed mo...

Journal: :Molecules 2015
Guillermo Soriano-Moro María Judith Percino Ana Laura Sánchez Víctor Manuel Chapela Margarita Cerón María Eugenia Castro

The synthesis and characterization of the precursor isomers trans-4-(2-(pyridin-2-yl)vinylbenzaldehyde (I), trans-4-(2-(pyridin-4-yl)vinylbenzaldehyde (II), trans-4-(2-(pyridin-2-yl)vinylbenzoic acid (III) and (E)-4-(2-(pydridin-4-yl)vinylbenzoic acid (IV) are reported. These compounds were prepared in order to obtain trans-4-((E)-2-(pyridin-2-yl)vinyl)benzamide-TEMPO (V). Compounds I and II we...

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