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A novel tandem process leading to functionalized glutarimides

Authorized Users Only
2005
Authors
Popović-Djordjević, Jelena
Ivanović, MD
Kiricojević, Vesna D.
Article (Published version)
Metadata
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Abstract
The synthesis of various functionalized or spirobicyclic glutarimides by a novel tandem process has been disclosed. The reaction involves a base-catalyzed Michael addition of active methylene compounds to secondary conjugated amides, followed by intramolecular N-acylation of the carboxamido group. It provides a relatively general and simple access to useful synthetic intermediaries and potentially active pharmacological compounds. In addition, a novel group of spirobicyclic systems has been synthesized.
Keywords:
synthesis / functionalized or spirobicyclic glutarimides / tandem process
Source:
Tetrahedron Letters, 2005, 46, 15, 2611-2614
Publisher:
  • Pergamon-Elsevier Science Ltd, Oxford

DOI: 10.1016/j.tetlet.2005.02.087

ISSN: 0040-4039

WoS: 000228115600019

Scopus: 2-s2.0-15244347524
[ Google Scholar ]
8
7
URI
http://aspace.agrif.bg.ac.rs/handle/123456789/1022
Collections
  • Radovi istraživača / Researchers’ publications
Institution/Community
Poljoprivredni fakultet
TY  - JOUR
AU  - Popović-Djordjević, Jelena
AU  - Ivanović, MD
AU  - Kiricojević, Vesna D.
PY  - 2005
UR  - http://aspace.agrif.bg.ac.rs/handle/123456789/1022
AB  - The synthesis of various functionalized or spirobicyclic glutarimides by a novel tandem process has been disclosed. The reaction involves a base-catalyzed Michael addition of active methylene compounds to secondary conjugated amides, followed by intramolecular N-acylation of the carboxamido group. It provides a relatively general and simple access to useful synthetic intermediaries and potentially active pharmacological compounds. In addition, a novel group of spirobicyclic systems has been synthesized.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - A novel tandem process leading to functionalized glutarimides
EP  - 2614
IS  - 15
SP  - 2611
VL  - 46
DO  - 10.1016/j.tetlet.2005.02.087
ER  - 
@article{
author = "Popović-Djordjević, Jelena and Ivanović, MD and Kiricojević, Vesna D.",
year = "2005",
abstract = "The synthesis of various functionalized or spirobicyclic glutarimides by a novel tandem process has been disclosed. The reaction involves a base-catalyzed Michael addition of active methylene compounds to secondary conjugated amides, followed by intramolecular N-acylation of the carboxamido group. It provides a relatively general and simple access to useful synthetic intermediaries and potentially active pharmacological compounds. In addition, a novel group of spirobicyclic systems has been synthesized.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "A novel tandem process leading to functionalized glutarimides",
pages = "2614-2611",
number = "15",
volume = "46",
doi = "10.1016/j.tetlet.2005.02.087"
}
Popović-Djordjević, J., Ivanović, M.,& Kiricojević, V. D.. (2005). A novel tandem process leading to functionalized glutarimides. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford., 46(15), 2611-2614.
https://doi.org/10.1016/j.tetlet.2005.02.087
Popović-Djordjević J, Ivanović M, Kiricojević VD. A novel tandem process leading to functionalized glutarimides. in Tetrahedron Letters. 2005;46(15):2611-2614.
doi:10.1016/j.tetlet.2005.02.087 .
Popović-Djordjević, Jelena, Ivanović, MD, Kiricojević, Vesna D., "A novel tandem process leading to functionalized glutarimides" in Tetrahedron Letters, 46, no. 15 (2005):2611-2614,
https://doi.org/10.1016/j.tetlet.2005.02.087 . .

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