Ring Annulation Versus Alkylation of Pyrrole With Α-Phosphoryl Ketones
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Date
2016
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Pergamon-elsevier Science Ltd
Open Access Color
Green Open Access
No
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Publicly Funded
No
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).
WoS Q
Q2
Scopus Q
Q3

OpenCitations Citation Count
6
Source
Tetrahedron
Volume
72
Issue
39
Start Page
5934
End Page
5942
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Citations
CrossRef : 3
Scopus : 6
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