The rapid growth of the biodiesel industry has led to a large surplus of its major byproduct, i.e. glycerol, for which new applications need to be found. Research efforts in this area have focused mainly on the development of processes for converting glycerol into value-added chemicals and its reforming for hydrogen production, but recently, in line with the increasing interest in the use of alternative greener solvents, an innovative way to revalorize glycerol and some of its derivatives has seen the light, i.e. their use as environmentally friendly reaction media for synthetic organic chemistry. The aim of the present Feature Article is to provide a comprehensive overview on the developments reached in this field.
Amides are versatile building blocks in synthetic organic chemistry, presenting a wide range of pharmacological applications, and are used as raw materials in industry for the large-scale production of engineering plastics, detergents and lubricants. The development of green procedures for the synthesis of this relevant class of compounds from various starting materials, which replace antiquated methods using carboxylic acid derivatives and amines, is therefore of prime interest in modern chemistry. In this review article, a survey of metal-catalyzed synthetic approaches of amides conducted in an environmentally friendly aqueous medium is given.
2 February 2001 in European Journal of Inorganic Chemistry
The catalytic isomerization of propargylic alcohols promoted by transition-metals represents a straightforward and appealing route to synthetically useful α,β-unsaturated carbonyl compounds. Three different reaction pathways are known for these atom-economical transformations: (i) the so-called Meyer–Schuster and Rupe rearrangements, in which a formal 1,3- or 1,2-shift of the hydroxyl group takes place, and (ii) the redox-type isomerization, which involves a simultaneous oxidation of the alcohol unit and reduction of the CC bond. In this Perspective article an overview of the different metal catalysts presently available to promote these isomerization reactions, their mechanisms of action as well as relevant synthetic applications, is provided.