Esterification of several carboxylic acids with supercritical alcohols such as 1-propanol, 1butanol, 1-octanol, isoamylalcohol, ethanol, methanol, and subcritical benzyl alcohol without using any catalyst was studied. A variety of esters were synthesized very effectively using supercritical alcohols as solvent and reagent. Moderate to excellent yields were obtained depending on the nature of th...

Iridium catalysts supported on anatase with high surface area showed excellent activities for the acceptor-less dehydrogenation synthesis of benzoxazoles from 2-aminophenol and primary alcohols. The catalytic activity greatly depended titania supports, iridium precursors, loading species. Catalysts JRC (Japan Reference Catalyst)-TIO-10 highest dehydrogenative reaction. Preparation using [Ir(cod...

Since alcohols are accessible from indigestible biomass (lignocellulose), the development of novel preferentially catalytic reactions in which alcohols are converted into important classes of fine chemicals is a central topic of sustainable synthesis. Multicomponent reactions are especially attractive in organic chemistry as they allow the synthesis of large libraries of diversely functionalize...

Bestmann ylide [(triphenylphosphoranylidene)ketene] acts as a chemical linchpin that links nucleophilic entities, such as alcohols or amines, with carbonyl moieties to produce unsaturated esters and amides, respectively. In this work, the formation of α,β,γ,δ-unsaturated esters (dienoates) is achieved through the coupling of Bestmann ylide, an alcohol and an α,β-unsaturated aldehyde. Primary an...

Enantiomerically pure secondary alcohols are essential compounds in organic synthesis and are used as chiral auxiliaries and synthetic intermediates in the pharmaceutical, agrochemical, and fine chemical industries. One of the attractive and practical approaches to achieving optically pure secondary alcohols is oxidative kinetic resolution of racemic secondary alcohols using chiral Mn(III) sale...

The stereocontrol of tertiary alcohols represents a recurrent challenge in organic synthesis. In the present paper, we describe simple, efficient, and indirect method to enantioselectively prepare through chiral isothiourea catalyzed selective acylation adjacent secondary alcohols. This transformation enables kinetic resolution (KR) easily prepared racemic diastereoenriched secondary/tertiary d...

Temperature programed desorption has been used to study the desorption kinetics and desorption energies of a set of alcohols and fluorinated alcohols adsorbed on an a-CHx film. The alcohols serve as models for the hydroxyl end groups of Fomblin Zdol, the lubricant most commonly used with the amorphous carbon overcoats sputtered onto the surfaces of magnetic data storage disks. Temperature progr...

Alcohol dehydrogenation and condensation reactions are involved in chain growth pathways on Cu/MgCeOx promoted with potassium. These pathways lead to the formation of isobutanol with high selectivity via reactions of higher alcohols with methanol-derived C1 species in reaction steps also relevant to higher alcohol synthesis from CO/H2 mixtures at higher pressures on K–Cu/MgCeOx catalysts. Ethan...

The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents to ketones is of central importance in organic chemistry. The resulting quaternary stereocentres are difficult to prepare selectively by other means despite their widespread occurrence in natural products and pharmaceuticals. Here we report on a new methodology which allows access to both α-bromo-...