18982-18-8Relevant articles and documents
Production of carboxylic acid and carboxylic acid ester allylation intermediate
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Paragraph 0071; 0072, (2019/06/04)
The invention discloses a preparation method of aryl/alkyl carboxylic acid which serves as a useful intermediate of a polymerized liquid crystal compound and is provided with (methyl) propene acyloxy, and aryl/alkyl allyl carboxylate which serves as an in
METHOD FOR MANUFACTURING P-HYDROXY BENZOIC ACID ALLYL POLYMER
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Paragraph 0049, (2017/02/24)
PROBLEM TO BE SOLVED: To provide a method for efficiently manufacturing p-hydroxy benzoic acid allyl polymer having high antibacterial property. SOLUTION: There is provided a method for manufacturing p-hydroxy benzoic acid allyl polymer including (A) a pr
A simple FRET-based modular design for diagnostic probes
Redy, Orit,Kisin-Finfer, Einat,Sella, Eran,Shabat, Doron
supporting information; scheme or table, p. 710 - 715 (2012/02/05)
In recent years, there has been a massive effort to develop molecular probes with optical modes of action. Probes generally produce detectable signals based on changes in fluorescence properties. Here, we demonstrate the potential of self-immolative molecular adaptors as a platform for Turn-On probes based on the FRET technique. The probe is equipped with identical fluorophore pairs or a fluorophore/quencher FRET pair and a triggering substrate. Upon reaction of the analyte of interest with the triggering substrate, the self-immolative adaptor spontaneously releases the two dye molecules to break off the FRET effect. As a result, a new measurable fluorescent signal is generated. The fluorescence obtained can be used to quantify the analyte. The modular structure of the probe design will allow the preparation of various chemical probes based on the FRET activation technique.
(Meth)acrylate compound, curable composition using the same, curable composition for photo-nanoimprints, cured product of curable composition and method for manufacturing cured product
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Page/Page column 34, (2012/11/06)
It's object is to provide a (meth)acrylate compound excellent in photocurability, a curable composition comprising the compound and excellent in all of pattern accuracy, peelability, surface hardness, elasticity recovery and solvent resistance, an optical
Synthesis of para-substituted bicyclo[2.2.1]hept-5-en-2-ylmethyl benzoates
Mamedbeili,Kyazimova,Nagiev,Abdiev,Aliev
experimental part, p. 74 - 77 (2009/07/17)
para-Substituted bicyclo[2.2.1]hept-5-en-2-ylmethyl benzoates were synthesized by the Diels-Alder reaction of cyclopentadiene with the corresponding para-substituted allyl benzoates, and optimal reaction conditions were found. The product structure was confirmed by independent synthesis and IR and 1H NMR spectroscopy.
Synthesis and photostabilizing properties of hexachlorobicyclo[2.2.1]hept- 5-enylmethyl esters of substituted benzoic acids
Kyazimova,Mamedov,Babaev,Mamedova
, p. 438 - 442 (2008/09/20)
Polychlorinated bicyclic esters of p-substituted benzoic acids were prepared by the Diels-Alder reaction of hexachlorocyclopentadiene with allyl esters of p-substituted benzoic acids. Some of the adducts synthesized were tested as photostabilizers for polyethylene-based polymer formulations.
Synthesis of novel aromatic macrolactones via ring closing metathesis of substituted phenylalkanoic acid allylic esters
Brown, David P.,Duong, Hoan Q.
, p. 435 - 443 (2008/09/19)
(Chemical Equation Presented) Stable aromatic macrolactones have been synthesized and characterized from 2- and 3-substituted phenylalkanoic acid systems in modest yields.
Design and synthesis of phosphotyrosine peptidomimetic prodrugs
Garrido-Hernandez, Hugo,Moon, Kyung D.,Geahlen, Robert L.,Borch, Richard F.
, p. 3368 - 3376 (2007/10/03)
A novel approach to the intracellular delivery of aryl phosphates has been developed that utilizes a phosphoramidate-based prodrug approach. The prodrugs contain an ester group that undergoes reductive activation intracellularly with concomitant expulsion
Allylation of Alcohols and Carboxylic Acids with Allyl Acetate Catalyzed by [Ir(cod)2]+BF4- Complex
Nakagawa, Hideto,Hirabayashi, Tomotaka,Sakaguchi, Satoshi,Ishii, Yasutaka
, p. 3474 - 3477 (2007/10/03)
A facile method for the synthesis of allyl alkyl ethers from alcohols with allyl acetate was developed by the use of [Ir(cod)2] +BF4- complex. For instance, the reaction of allyl acetate with n-octyl alcohol in the presence of a catalytic amount of [Ir(cod)2]+BF4- complex afforded allyl octyl ether in quantitative yield. Allyl carboxylates were also prepared by the exchange reaction between carboxylic acids and allyl acetate in good yields. The [Ir(cod)2]+BF4- complex catalyzed the reaction of alkyl and aromatic amines with allyl acetate to lead to the corresponding allylamines in fair to good yields.