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<title>Kimya Bilim Dalı</title>
<link>http://hdl.handle.net/20.500.12416/2168</link>
<description>Kimya Bilim Dalı makalelerini içerir.</description>
<pubDate>Wed, 28 Oct 2026 16:43:20 GMT</pubDate>
<dc:date>2026-10-28T16:43:20Z</dc:date>
<item>
<title>Ring annulation versus alkylation of pyrrole with alpha-phosphoryl-alpha,beta-unsaturated ketones</title>
<link>http://hdl.handle.net/20.500.12416/3385</link>
<description>Ring annulation versus alkylation of pyrrole with alpha-phosphoryl-alpha,beta-unsaturated ketones
Taşgın, Dilek Işık; Unaleroğlu, Canan
In this study; novel aryl, heteroaryl, pyrrolyl and phosphoryl groups containing pyrrolizines were synthesized by the ring annulation reaction of aryl or heteroaryl substituted alpha-phosphoryl-alpha,beta-unsaturated ketones with pyrrole under mild reaction conditions. This domino reaction involves scandium triflate catalyzed addition of pyrrole to the double bond of alpha-phosphoryl-alpha,beta-unsaturated ketones, carbonyl group and finally ring annulation sequences. The presented work provided a convenient way for the synthesis of novel bispyrrolic compounds. (C) 2016 Elsevier Ltd. All rights reserved.
</description>
<pubDate>Thu, 29 Sep 2016 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/20.500.12416/3385</guid>
<dc:date>2016-09-29T00:00:00Z</dc:date>
</item>
<item>
<title>N-phosphorylation of pyrroles: An intramolecular migration reaction</title>
<link>http://hdl.handle.net/20.500.12416/1828</link>
<description>N-phosphorylation of pyrroles: An intramolecular migration reaction
Taşgın, Dilek; Unaleroğlu, Canan
A new synthetic method is reported for the N-phosphorylation of pyrroles via intramolecular migration of a phosphonate diester group. The reaction proceeds under mild conditions and produces N-phosphorylated pyrrole derivatives in moderate to good yields.
</description>
<pubDate>Wed, 16 May 2018 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/20.500.12416/1828</guid>
<dc:date>2018-05-16T00:00:00Z</dc:date>
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