65409-15-6Relevant academic research and scientific papers
Long conjugated 2-nitrobenzyl derivative caged anticancer prodrugs with visible light regulated release: Preparation and functionalizations
Bao, Chunyan,Jin, Ming,Li, Bo,Xu, Yaodong,Jin, Jingyan,Zhu, Linyong
, p. 5238 - 5244 (2012/08/08)
A series of anticancer prodrugs with different chemical functional groups were prepared, in which the styryl conjugated 2-nitrobenzyl derivatives were introduced as the phototrigger to regulate the drug (chlorambucil) release. Compared to the common 4,5-dimethoxy-2-nitrobenzyl caged compounds, most of the prodrugs exhibited large and redshifted one-photon absorption within the visible range. One-photon excitation for the drug release was studied by measuring UV-vis absorption, FT-IR, and HPLC spectra, which suggested that chlorambucil was released effectively and precisely by manipulating external light conditions. And the introduction of different functional groups made this type of prodrug a good platform to further react with some typical drug carriers and to further form excellent visible light responsive drug delivery systems. Moreover, the drug also could be effectively released under the excitation of two-photon at 800 nm with comparable photorelease efficiencies. The Royal Society of Chemistry 2012.
Rhodium-catalyzed synthesis of terminal alkenes
Paquet, Valerie,Lebel, Helene
, p. 1901 - 1905 (2007/10/03)
Terminal alkenes have been efficiently prepared via a rhodium-catalyzed olefination procedure using Wilkinson's catalyst in the presence of triphenylphosphine, 2-propanol and trimethylsilyldiazomethane. Optimized reaction conditions are described for aldehydes and ketones, as well as alternative work up procedures. Georg Thieme Verlag Stuttgart.
Rhodium-Catalyzed Methylenation of Aldehydes
Lebel, Helene,Paquet, Valerie
, p. 320 - 328 (2007/10/03)
The rhodium-catalyzed methylenation of aldehydes using trimethylsilyldiazomethane and triphenylphosphine produces a variety of terminal alkenes in excellent yields. These mild and nonbasic reaction conditions allow the conversion of enolizable substrates (keto aldehydes and nonracemic α-substituted aldehydes) to terminal alkenes without epimerization. Optimization of the reaction conditions led to the conclusion that a variety of rhodium(I) sources can be used as catalysts. The effect of the solvent on the reaction has also been studied, and it indicates that although the THF is the best solvent, other solvents may be used. The reactivity of the system is very much dependent on the nature of the phosphine reagent. The use of an easily removable phosphine is also described. Spectroscopic studies indicate that the reaction proceeds via an unusual mechanism which leads to the in situ formation of the salt-free phosphorus ylide, methylenetriphenylphosphorane.
Design and biological evaluation of non-peptide analogues of omega-conotoxin MVIIA
Menzler, Stefan,Bikker, Jack A.,Suman-Chauhan, Nirmala,Horwell, David C.
, p. 345 - 347 (2007/10/03)
Omega-conotoxin MVIIA, a highly potent antagonist of the N-type voltage sensitive calcium channel, has shown utility in several models of pain and ischemia. We report a series of three alkylphenyl ether based analogues which mimic three key amino acids of the toxin. Two of the compounds have been found to exhibit IC50 values of 2.7 and 3.3 μM at the human N-type voltage sensitive calcium channel. (C) 2000 Elsevier Science Ltd. All rights reserved.
Certain 4-cyclopropylphenyl geranyl ethers and their use in controlling insects
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, (2008/06/13)
Compounds which are useful for controlling insects by impeding their metamorphosis, have the formula STR1 wherein i. A and B together form a bond, II. A and B together form an epoxide link, Or Iii. A is hydrogen and B is C1 -C4 alkox
