A novel tandem process leading to functionalized glutarimides
Samo za registrovane korisnike
2005
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
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. (c) 2005 Elsevier Ltd. All rights reserved.
Ključne reči:
synthesis / functionalized or spirobicyclic glutarimides / tandem processIzvor:
Tetrahedron Letters, 2005, 46, 15, 2611-2614Izdavač:
- Oxford : Pergamon-Elsevier Science Ltd
DOI: 10.1016/j.tetlet.2005.02.087
ISSN: 0040-4039
WoS: 000228115600019
Scopus: 2-s2.0-15244347524
Institucija/grupa
IHTMTY - JOUR AU - Popović-Đorđević, Jelena B. AU - Ivanović, Milovan D. AU - Kiricojević, Vesna PY - 2005 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/2678 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. (c) 2005 Elsevier Ltd. All rights reserved. PB - Oxford : Pergamon-Elsevier Science Ltd T2 - Tetrahedron Letters T1 - A novel tandem process leading to functionalized glutarimides VL - 46 IS - 15 SP - 2611 EP - 2614 DO - 10.1016/j.tetlet.2005.02.087 ER -
@article{ author = "Popović-Đorđević, Jelena B. and Ivanović, Milovan D. and Kiricojević, Vesna", 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. (c) 2005 Elsevier Ltd. All rights reserved.", publisher = "Oxford : Pergamon-Elsevier Science Ltd", journal = "Tetrahedron Letters", title = "A novel tandem process leading to functionalized glutarimides", volume = "46", number = "15", pages = "2611-2614", doi = "10.1016/j.tetlet.2005.02.087" }
Popović-Đorđević, J. B., Ivanović, M. D.,& Kiricojević, V.. (2005). A novel tandem process leading to functionalized glutarimides. in Tetrahedron Letters Oxford : Pergamon-Elsevier Science Ltd., 46(15), 2611-2614. https://doi.org/10.1016/j.tetlet.2005.02.087
Popović-Đorđević JB, Ivanović MD, Kiricojević V. 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-Đorđević, Jelena B., Ivanović, Milovan D., Kiricojević, Vesna, "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 . .