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Ring Annulation Versus Alkylation of Pyrrole With Α-Phosphoryl Ketones

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Date

2016

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Volume Title

Publisher

Pergamon-elsevier Science Ltd

Open Access Color

Green Open Access

No

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Abstract

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

Keywords

Pyrrolizines, Phosphonates, Ring Annulation, Michael Addition

Turkish CoHE Thesis Center URL

Fields of Science

01 natural sciences, 0104 chemical sciences

Citation

Tasgin, Dilek Isik; Unaleroglu, Canan, "Ring annulation versus alkylation of pyrrole with alpha-phosphoryl-alpha,beta-unsaturated ketones", Tetrahedron, Vol. 72, No. 39, pp. 5934-5942, (2016).

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Q2

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Q3
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OpenCitations Citation Count
6

Source

Tetrahedron

Volume

72

Issue

39

Start Page

5934

End Page

5942
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CrossRef : 3

Scopus : 6

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Mendeley Readers : 6

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