نتایج جستجو برای: acylals

تعداد نتایج: 30  

[B(OH)3]0.78[B(OH)2(OSO3H)]0.22 or (BSA) was simply prepared by addition of chlorosulfonic acid to commercial boric acid at room temperature. This cheap and green solid acid was used as an efficient catalyst for synthesis of acylals from aldehydes under solvent-free conditions at room temperature.

Nano-silica supported boron trifluoride (BF3.SiO2) is an efficient, reusable and eco-friendly catalyst for chemoselective thioacetalization of aldehydes and ketones. So, this catalyst was applied for transthioacetalization of acetals and acylals into their corresponding 1,3-dithiolanes or 1,3-dithianes  in good to excellent yields. The reactions were carried out at room temperature under solven...

Journal: :iranian journal of science and technology (sciences) 2013
a. z. sardarian

4-dodecylbenzenesulfonic acid (dbsa) has been shown to be an efficient, mild, green, stable and chemoselective brønsted acid catalyst for the synthesis of 1, 1-diacetates (acylals) of aldehydes under solvent-free conditions. the mild condition, eco-friendly, excellent yields, short reaction times and using an easily available, inexpensive and reusable catalyst are important features of this met...

Journal: :iranian journal of science and technology (sciences) 2015
s. rezayati

an efficient and chemoselective procedure for the preparation of 1, 1-diacatates (acylals) from various aldehydes with acetic anhydride in the presence of brønsted acidic ionic liquid [msei]cl as a reusable catalytic system under solvent-free condition at room temperature and short periods of times with excellent yields will be described. the catalyst was easily separated in simple work-up and ...

Journal: :The Journal of biological chemistry 1988
R Wolfenden Y L Liang

When carbohydrates in aqueous solution combine with biological receptors, their interactions with the binding site take the place of previous interactions with solvent water. Free energies of binding can therefore be considered to depend on free energies of solvation of the interacting partners before and after complexation. Because carbohydrates contain so many polar substituents, their overal...

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