Novel Selenium-Mediated Rearrangements and Cyclisations, 2013 Springer Theses Series, Vol. 77

In his thesis, Sohail Shahzad carefully investigates carbon nucleophiles in selenocyclisations, as well as reaction protocols for performing such reactions catalytically. After a comprehensive introduction to the element selenium, the author goes on to report the synthesis of several substrates for carbocyclisation reactions and the use of selenium reagents for the preparation of dihydronaphthalenes. Further chapters detail electrophilic selenium-mediated reactions, and novel strategies using selenium catalysts together with stoichiometric amounts of hypervalent iodine reagents as oxidants to convert stilbene carbosylic acids into the corresponding isocoumarins. This thesis outlines some excellent new synthetic routes which will be useful tools for synthetic organic chemistry in the future.

General Introduction on Selenium.- The Synthesis of Novel Dihydronaphthalenes and Benzofluorenes.- The Synthesis of Naphthalenes and Biaryls.- Synthesis of Isocoumarins and Dihydroisocoumarins.- Experimental Section.

Nominated by the University of Cardiff as an outstanding PhD thesis Careful investigation of carbon nucleophiles in selenocyclizations Description and development of excellent new synthetic routes Includes supplementary material: sn.pub/extras