Nowadays, chirality is widely accepted as an important factor in
molecular recognition processes and the biological activity of many
pharmaceutical drugs and agrochemicals; this is confirmed by the
continuous need for synthetic methods which lead to single or enriched
enantiomers of such compounds. By presenting a review of the various and
more recently developed approaches for both metal-transition and
organocatalysis, this volume describes the development of "greener"
asymmetric reactions which preserve stereoselectivity. The author
summarizes the impressive amount of research that has been gathered
within this field into three chapters focusing on: i)the search of
alternative catalysts, ii) alternative solvents, and iii) alternative
synthetic strategies and processes. For each topic, the fundamentals and
some valuable applications are discussed.