Selective oxidation of the so-called fatty alcohols, aliphatic long chain alcohols that are present in vegetable waxes, forestry residues and pulping industry subproducts, could be used to obtain the corresponding aldehydes, acids and esters, widely used in pharmaceutical and cosmetic applications and as emulsifiers. The physico-chemical characteristics of this type of alcohols entail specific challenges for the reaction. This work is aimed to review and evaluate the state-of-art of catalytic selective oxidation of the higher fatty alcohols (C 10+), to assess the feasibility of new "green" processes using biomass for the production of fine chemicals. Due to the scarcity of information available on these reactions, the scope was extended to all C 8+ primary alkanols, to identify trends and characteristics of the oxidation of longer chain aliphatic alcohols, as well as suitable process conditions. The critical evaluation of available literature allows to conclude that the oxidation of higher alcohols is feasible using non enzymatic heterogeneous catalysts, either without solvent or with solvents miscible with both polar and nonpolar media (depending on the alcohol chain length), and using clean oxidants such as H 2 O 2 , molecular oxygen or air. The appropriate selection of the catalytic system and solvent may allow directing the reaction selectively to production of the aldehyde, the acid or the ester. These features would allow the implementation of small-scale processes, well in accordance with the principles of "green chemistry".

There is a small percentage of adults with IBD at risk of primary EBV infection. The risks of seroconversion and its complications remain through adulthood. Our results suggest that, when considering the use of thiopurines in IBD, the information on EBV serological status should be taken into account at any age.

No abstract

No abstract