Fr. 135.00

Novel Selenium-Mediated Rearrangements and Cyclisations

English · Paperback / Softback

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Description

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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.

List of contents

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

Summary

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.

Product details

Authors Sohail Anjum Shahzad
Publisher Springer, Berlin
 
Languages English
Product format Paperback / Softback
Released 01.01.2014
 
EAN 9783642428746
ISBN 978-3-642-42874-6
No. of pages 192
Dimensions 155 mm x 11 mm x 235 mm
Weight 330 g
Illustrations XX, 192 p.
Series Springer Theses
Springer Theses
Subjects Natural sciences, medicine, IT, technology > Chemistry > Organic chemistry

Chemie, Anorganische Chemie, B, ORGANIC CHEMISTRY, chemistry, Chemistry and Materials Science, Chemistry/Food Science, general, Inorganic Chemistry, Selenium-Mediated Rearrangements, Friedel-Crafts Acylations, Selenium Electrophiles, Diselenide Catalyzed O-Cyclizations

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