نتایج جستجو برای: preparation of alcohols

تعداد نتایج: 21170995  

Journal: :polyolefins journal 2015
toshiaki funako patchanee chammingkwan toshiaki taniike minoru terano

in ziegler-natta olefin polymerization, the pore architecture of catalysts plays a crucial role in catalyticperformances and polymer properties. while the type of preparation routes (such as chemical reaction andsolution precipitation) greatly affects the catalyst pore architecture as a result of different solidification mechanisms,the modification of the pore architecture within a given route ...

Journal: :iranian journal of catalysis 2015
najme kalvari janaki razieh fazaeli hamid aliyan

a series of fe3o4 supported on mesoporous fdu-12 silica systems were prepared by the hydrothermal conditions. the surface properties of the functionalized catalyst were analyzed by a series of characterization techniques like ftir, xrd, n2 adsorption–desorption and tem. xrd and adsorption–desorption analysis shows that the mesostructure of fdu silica remains intact after fe3o4 modifications, wh...

Journal: :The Journal of pharmacology and experimental therapeutics 1997
X L Zheng S Mokashi M D Hollenberg

We observed a contractile action of ethanol (20-500 mM) and other alcohols (methanol and propanol, but not butanol) in guinea pig gastric longitudinal (LM) and circular (CM) smooth muscle preparations. The potency order for the alcohols in the LM preparation was: ethanol = propanol > methanol; and in the CM preparation, propanol > ethanol > methanol. Like epidermal growth factor-urogastrone (EG...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2009
m. majid heravi sodeh sadjadi rahim hekmatshoar hossein abdi oskooie fatemeh bamoharram

the catalytic air oxidation-trimerization of alcohols was carried out with hetropolyacids. in the presence of hetropolyacid formation of cyclotrimers of alcohols and aldol condensation products was observed. the 1,3,5-trioxanes were major and aldol condensation compounds were minor products.

2018
Jie Li Bihui Zhou Yajie Jiang Xiaoming Liu

A concise method for the preparation of new 3,4,5,6-tetrahydropyrimidinium salts was presented in this paper. Further application of these salts in asymmetric diethylzinc addition of arylaldehydes was explored, giving the corresponding chiral second alcohols in good yields and moderate enantioselectivities.

Journal: :physical chemistry research 2016
forough kalantari fotooh maryam baharizadeh

oniom calculation is carried out to estimate the acidity of five aliphatic alcohols before and after adsorbing on the tip of (8,0) single-walled carbon nanotube. the oniom method is performed using a combination of density functional theory and am1 semiemperical method for alcohols and their corresponding conjugated bases. deprotonation gibbs free energies of alcohols are calculated and compare...

Journal: :Organic letters 2012
Hogyu Lee Jun Hee Kim Won Koo Lee Jae-Hoon Jung Hyun-Joon Ha

A new and efficient preparation of pharmacologically and biologically important 2,5-disubstituted 6-azaindoles was achieved from cyclizations of aziridin-2-yl dipropargylic alcohols as adducts of two propargyl groups to ethyl 1-benzylaziridine-2-carboxylate. The sequential cyclizations include pyrrole formation and a novel base-catalyzed intramolecular acetylenic Schmidt reaction.

Journal: :Organic & biomolecular chemistry 2012
R Adam Mosey Paul E Floreancig

A series of α-alkoxy carbamates that cleave under mild conditions to release alcohols has been synthesized through a multicomponent process. The relationship between structural features in these compounds and the rate of alcohol release in the presence of basic hydrogen peroxide has been studied. The preparation of carbamates that cleave under other conditions has been demonstrated.

Journal: :Chemical communications 2012
Jun Zhang Xiaolong Su Jun Fu Xinke Qin Meixin Zhao Min Shi

We have found a Tf(2)O-mediated intramolecular cyclization reaction and have revealed an intriguing stereoselectivity and a regioselectivity during the preparation of intermediate alcohols, which allow for the tailor-made synthesis of various backbone-substituted imidazolinium salts, and structurally specific syn-4,5-disubstituted imidazolinium salts.

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