Titlebook: Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis o; Robert Doran Book 2015 The Editor(s)

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M. Ataharul Islam,Abdullah Al-Shihaylative protonation of the corresponding α-aryl-β-keto allyl esters. Enantioselectivities of up to 92 % . and 74 % . were achieved for cyclopentanone and cyclohexanone substrates, respectively. The route described gives access to these important structural motifs in moderate to high levels of enanti

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,Introduction to the Development of a Catalytic Asymmetric Synthesis of Tertiary α-Aryl Ketones,Biological systems recognise a pair of enantiomers as different substances and thus each enantiomer will trigger a different response. It is possible that one enantiomer could act positively as a therapeutic agent and the other enantiomer might be very harmful or toxic.

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Robert DoranNominated as an outstanding Ph.D. thesis by University College Dublin, Ireland.Outlines the synthesis of a new bioactive lactone-containing natural product analog.Describes the development of a cataly

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