Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
An Approach to the synyhesis of novel pyrrole fused heterocycles
Download
index.pdf
Date
2016
Author
Öztürk, Uğur Başak
Metadata
Show full item record
Item Usage Stats
246
views
100
downloads
Cite This
Pyrrole and pyrrole derivatives are prominent building blocks in organic synthesis due to their biological activities and natural occurrence. For the formation of pyrrole derivatives, electrophilic cyclizations are considered efficient and significant processes. In this thesis, novel N-alkynyl-2-phenyl-substituted pyrrole derivatives were synthesized and electrophilic cyclization reactions of these compounds were investigated. Catalyst such as AuCl3, AuBr3, I2, ICl, FeCl3, InCl3 and Cu(OTf)2 were used for the ring closure studies.
Subject Keywords
Pyrroles.
,
Electrophiles.
,
Heterocyclic compounds.
,
Ring formation (Chemistry).
URI
http://etd.lib.metu.edu.tr/upload/12619872/index.pdf
https://hdl.handle.net/11511/25521
Collections
Graduate School of Natural and Applied Sciences, Thesis
Suggestions
OpenMETU
Core
The Synthesis of 6- and 7- membered heterocyclic ring systems fused to pyridine ring
Dinçoflaz, Yasemin; Balcı, Metin; Department of Chemistry (2013)
The synthesis of the nitrogen containing heterocyclic compounds is one of the leading research areas throughout the organic chemistry due to their significant activities in biological systems. Among the various biologically active molecules, pyridine-fused ring systems are of prime importance on the grounds of their proven clinical roles. The coupling reactions with 6-membered heterocyclic compounds and diazepines gave rise to new pharmalogical compounds in recent years. Therefore, our object was the synthe...
A COMPUTATIONAL STUDY ON SOME SELENIUM-CONTAINING NAPHTHALENE DERIVATIVES
Türker, Burhan Lemi (Informa UK Limited, 2009-01-01)
A quantum chemical study, based on DFT theory is presented which considers certain selenium-containing naphthalene derivatives, including a keto group together with a Se atom embedded in either a five- or six-membered ring fused with naphthalene moiety. The corresponding enol structures also are considered. The quantum chemical and IR data collected are analyzed and NICS(0) values have been obtained.
Synthesis of indole fused heterocyclic compounds
Kaptı, Tolga; Balcı, Metin; Department of Chemistry (2013)
Nitrogen containing heterocyclic compounds show wide range of biological activities so their syntheses have always been attractive area in organic chemistry. Indole derivatives, which are one of the important example of these biological active compound, are precursors to many pharmaceuticals. The aim of this research is to develop new synthetic methodologies leading to the synthesis of new derivatives of pyrimidoindole and quinoline, which have been found to show important biological activities. In this stu...
A new strategy for the synthesis of pyridines from N-propargylic beta-enaminothiones
Kelgokmen, Yilmaz; Zora, Metin (Royal Society of Chemistry (RSC), 2019-03-07)
A new method for the synthesis of 2,4,5-trisubstituted pyridines from N-propargylic beta-enaminothiones is reported. beta-Enaminothiones were prepared by thionation of the corresponding beta-enaminones with Lawesson's reagent. When treated with diisopropylamine in DMF at room temperature, N-propargylic beta-enaminothiones yielded 2,4,5-trisubstituted pyridines in moderate to high yields, along with small amounts of 2-methylene-2,3-dihydro-1,4-thiazepines. The reaction was found to be general for a broad ran...
Development of new synthetic methodologies for indole derivatives
Kılıklı, Ahmet Alper; Balcı, Metin; Department of Chemistry (2010)
Synthesizing nitrogen containing heterocyclic compounds is one of the leading research areas throughout the organic chemistry due to their significant activities on biological systems. Among the various biologically active molecules, indole derivatives are of prime importance on the grounds of their proven clinical roles. Objective of this study is to synthesize new indole derivatives those may contribute treatment of several diseases like their analogues via a recently developed synthetic methodology. Besi...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
U. B. Öztürk, “An Approach to the synyhesis of novel pyrrole fused heterocycles,” M.S. - Master of Science, Middle East Technical University, 2016.