Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/99607
Title: Formation of carbon-carbon bond via nitroalkanes under heterogeneous catalyst
Other Titles: Recent research developments in organic chemistry
Authors: Ballini, Roberto
Bosica, Giovanna
Keywords: Heterogeneous catalysis
Nitroalkanes -- Synthesis
Carbonyl compounds
Chemistry, Organic
Organic compounds -- Synthesis
Issue Date: 1997
Publisher: Transworld Research Network
Citation: Ballini, R., & Bosica, G. (1997). Formation of carbon-carbon bond via nitroalkanes under heterogeneous catalyst. In S. G. Pandalai (Ed.), Recent research developments in organic chemistry (pp. 11-24). Trivandrum, India: Transworld Research Network.
Abstract: Nitroalkanes are very important starting material in the formation of carbon-carbon bond. Under basic conditions, the nitronate union can react with saturated or conjugated carbonyl compounds, nitroaldol (Henry) or Michael reaction, respectively, leading to 1,2- and 1,4-difunctionalized derivatives. These reactions are routinely performed under homogeneous solution of the reactants in an organic solvent using soluble bases, but, different drawbacks are often observed following these conditions. In the recent years there has been a tremendous upsurge of interest in various chemical transformations mediated by heterogeneous catalysis. In fact under heterogeneous catalyst chemical reactions can occur with better efficiency, higher purity of the products, and an easier work-up. In this context, recently, different heterogeneous catalyses have been successfully employed for the formation of C-C bond (Henry and Michael reaction) via nitroalkanes.
URI: https://www.um.edu.mt/library/oar/handle/123456789/99607
ISBN: 9788186846001
Appears in Collections:Scholarly Works - FacSciChe

Files in This Item:
File Description SizeFormat 
Formation_of_carbon_carbon_bond_via_nitroalkanes_under_heterogeneous_catalyst_1997.PDF
  Restricted Access
409.73 kBAdobe PDFView/Open Request a copy


Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.