Abstract
La(NO3)3.6H2O was used as an efficient catalyst for highly diastereoselective synthesis of functionalized piperidines by one-pot five-component reactions of anilines and aromatic aldehydes with acetoacetic esters. This strategy proceeds by way of the Knoevenagel reaction followed by inter-molecular aza-Diels-Alder reaction. The main features of the current method comprise mild reaction conditions, easy work-up, eco-friendliness, high atom economy, short times and the products were isolated with high yields.
Keywords: Lanthanum nitrate hexahydrate, piperidine, one-pot, multicomponent
Letters in Organic Chemistry
Title:La(NO3)3.6H2O Catalyzed One-pot Highly Diastereoselective Synthesis of Functionalized Piperidines
Volume: 10 Issue: 3
Author(s): Mir Rasul Mousavi, Jasem Aboonajmi, Malek Taher Maghsoodlou, Nourallah Hazeri, Sayyed Mostafa Habibi-Khorassani and Mohyeddin Safarzaei
Affiliation:
Keywords: Lanthanum nitrate hexahydrate, piperidine, one-pot, multicomponent
Abstract: La(NO3)3.6H2O was used as an efficient catalyst for highly diastereoselective synthesis of functionalized piperidines by one-pot five-component reactions of anilines and aromatic aldehydes with acetoacetic esters. This strategy proceeds by way of the Knoevenagel reaction followed by inter-molecular aza-Diels-Alder reaction. The main features of the current method comprise mild reaction conditions, easy work-up, eco-friendliness, high atom economy, short times and the products were isolated with high yields.
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Rasul Mousavi Mir, Aboonajmi Jasem, Taher Maghsoodlou Malek, Hazeri Nourallah, Mostafa Habibi-Khorassani Sayyed and Safarzaei Mohyeddin, La(NO3)3.6H2O Catalyzed One-pot Highly Diastereoselective Synthesis of Functionalized Piperidines, Letters in Organic Chemistry 2013; 10 (3) . https://dx.doi.org/10.2174/1570178611310030005
DOI https://dx.doi.org/10.2174/1570178611310030005 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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