Novel Selenium-Mediated Rearrangements and Cyclisations
Details
This book investigates carbon nucleophiles in selenocyclisations, as well as reaction protocols for performing such reactions catalytically. Details electrophilic selenium-mediated reactions and strategies using selenium catalysts and more.
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.
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
Inhalt
General Introduction on Selenium.- The Synthesis of Novel Dihydronaphthalenes and Benzofluorenes.- The Synthesis of Naphthalenes and Biaryls.- Synthesis of Isocoumarins and Dihydroisocoumarins.- Experimental Section.
Weitere Informationen
- Allgemeine Informationen
- GTIN 09783642331725
- Sprache Englisch
- Auflage 2013
- Genre Chemie
- Lesemotiv Verstehen
- Größe H241mm x B160mm x T17mm
- Jahr 2012
- EAN 9783642331725
- Format Fester Einband
- ISBN 3642331726
- Veröffentlichung 11.10.2012
- Titel Novel Selenium-Mediated Rearrangements and Cyclisations
- Autor Sohail Anjum Shahzad
- Untertitel Springer Theses 77
- Gewicht 489g
- Herausgeber Springer Berlin Heidelberg
- Anzahl Seiten 212