Novel selenium-mediated rearrangements and cyclisations

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...

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Détails bibliographiques
Auteur principal: Shahzad, Sohail Anjum, 19..-
Format: Livre numérique
Langue:Anglais
Publié: Berlin, Heidelberg : Springer Berlin Heidelberg [20..].
Cham : Springer Nature
Édition:1st ed. 2013.
Collection:Springer Theses, Recognizing Outstanding Ph.D. Research 77
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Edition sous un autre format:• Novel Selenium-Mediated Rearrangements and Cyclisations, Texte imprimé, 9783642331725
• Novel Selenium-Mediated Rearrangements and Cyclisations, Texte imprimé, 9783642331749
• Novel Selenium-Mediated Rearrangements and Cyclisations, Texte imprimé, 9783642428746
• Novel Selenium-Mediated Rearrangements and Cyclisations, Texte imprimé, 9783642331725
Description
Résumé: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
Description:Archives Springer e-books (Licence nationale)
Archives Springer e-books (Licence nationale)
ISBN:9783642331732
ISSN:2190-5061
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