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Transition Metal-Catalyzed Synthesis...

Pal, Arpan.

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Transition Metal-Catalyzed Synthesis and Applications of Enamino Carbonyl Compounds.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Transition Metal-Catalyzed Synthesis and Applications of Enamino Carbonyl Compounds./
Author:	Pal, Arpan.
Published:	Ann Arbor : ProQuest Dissertations & Theses, : 2019,
Description:	103 p.
Notes:	Source: Dissertation Abstracts International, Volume: 80-09(E), Section: B.
Contained By:	Dissertation Abstracts International80-09B(E).
Subject:	Chemistry. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=13880051
ISBN:	9781392148488

Transition Metal-Catalyzed Synthesis and Applications of Enamino Carbonyl Compounds.
Pal, Arpan.

Transition Metal-Catalyzed Synthesis and Applications of Enamino Carbonyl Compounds. - Ann Arbor : ProQuest Dissertations & Theses, 2019 - 103 p.

Source: Dissertation Abstracts International, Volume: 80-09(E), Section: B.

Thesis (Ph.D.)--The University of Tulsa, 2019.

Enaminones are valuable intermediates in organic synthesis. They have been used widely in the synthesis of pharmaceutically important heterocycles and natural products. In addition, there are many natural products that contain enaminone functional group. We have developed the sulfide contraction reaction of thioamides using acceptor/acceptor, acceptor-only and donor/acceptor substituted carbenoids to synthesize highly substituted enaminones. This method allows for the formation of cyclic, acyclic and chiral enaminones in moderate to excellent yields.

ISBN: 9781392148488Subjects--Topical Terms:

516420
Chemistry.

Transition Metal-Catalyzed Synthesis and Applications of Enamino Carbonyl Compounds.
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245 1 0 $a Transition Metal-Catalyzed Synthesis and Applications of Enamino Carbonyl Compounds.
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500 $a Source: Dissertation Abstracts International, Volume: 80-09(E), Section: B.
500 $a Adviser: Syed R. Hussaini.
502 $a Thesis (Ph.D.)--The University of Tulsa, 2019.
520 $a Enaminones are valuable intermediates in organic synthesis. They have been used widely in the synthesis of pharmaceutically important heterocycles and natural products. In addition, there are many natural products that contain enaminone functional group. We have developed the sulfide contraction reaction of thioamides using acceptor/acceptor, acceptor-only and donor/acceptor substituted carbenoids to synthesize highly substituted enaminones. This method allows for the formation of cyclic, acyclic and chiral enaminones in moderate to excellent yields.
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