A novel tandem process leading to functionalized glutarimides
Само за регистроване кориснике
2005
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
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.
Кључне речи:
synthesis / functionalized or spirobicyclic glutarimides / tandem processИзвор:
Tetrahedron Letters, 2005, 46, 15, 2611-2614Издавач:
- Pergamon-Elsevier Science Ltd, Oxford
DOI: 10.1016/j.tetlet.2005.02.087
ISSN: 0040-4039
WoS: 000228115600019
Scopus: 2-s2.0-15244347524
Колекције
Институција/група
Hemijski fakultet / Faculty of ChemistryTY - JOUR AU - Popović-Đorđević, Jelena AU - Ivanović, Milovan AU - Kiricojevic, VD PY - 2005 UR - https://cherry.chem.bg.ac.rs/handle/123456789/691 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 - Pergamon-Elsevier Science Ltd, Oxford 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 and Ivanović, Milovan and Kiricojevic, VD", 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 = "Pergamon-Elsevier Science Ltd, Oxford", 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., Ivanović, M.,& Kiricojevic, V.. (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-Đorđević J, Ivanović M, Kiricojevic 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, Ivanović, Milovan, Kiricojevic, VD, "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 . .