Νovel environmentally friendly organocatalytic and photoorganocatalytic transformations

Postgraduate Thesis uoadl:2775635 285 Read counter

Unit:
Κατεύθυνση Οργανική Σύνθεση και Εφαρμογές της στη Χημική Βιομηχανία
Library of the School of Science
Deposit date:
2018-06-26
Year:
2018
Author:
Spiliopoulou Nikoleta
Supervisors info:
Κόκοτος Χριστόφορος, Επίκουρος Καθηγητής, Τμήμα Χημείας, Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών
Original Title:
Ανάπτυξη καινοτόμων οργανοκαταλυτικών και φωτοοργανοκαταλυτικών μετασχηματισμών φιλικών προς το περιβάλλον
Languages:
Greek
Translated title:
Νovel environmentally friendly organocatalytic and photoorganocatalytic transformations
Summary:
Organocatalysis constitutes a new and fast moving catalysis’ field, which offers the opportunity of utilizing catalysts of low cost and environmentally friendly conditions for achieving a variety of asymmetric reactions. The first chapter of this thesis presents an introduction to Organocatalysis, while the second chapter refers to a literature survey on the applications of Organocatalysis in the enantioselective formation of α-chloro intermediates and expansion of Linchpin catalysis. The third chapter presents a review refers to organocatalysts for the aldol reactions and the fourth chapter refering to the Michael reaction. Photocatalysis is a new, interesting field which focuses on the use of irradiation as a source of energy. The fifth chapter of this thesis presents an introduction in Photochemistry and its applications in the synthesis of disulfides and creation new of C-N bonds. Finally, the sixth chapter presents a review in the organocatalytic oxidation method, which was developed in the Laboratory of Organic Chemistry of the National and Kapodistrian University of Athens, and refers to a literature report on oxidation methods for the synthesis of dihydrobenzofurans.
Main subject category:
Science
Keywords:
Organocatalysis, Photocatalysis, Aldol reaction, Morpholinones, Benzodihydrofurans
Index:
Yes
Number of index pages:
8
Contains images:
Yes
Number of references:
158
Number of pages:
90
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