Please use this identifier to cite or link to this item:
Title: Density functional study of 1,3-hydrogen shifts in 2,4-pyronone
Authors: Shukla, Piyush K
Singh, A
Mishra, S K
Ray, N K
Issue Date: Apr-2006
Publisher: NISCAIR-CSIR, India
Abstract: Density functional calculations have been performed to study 1,3 hydrogen shifts in 2,4-pyronone. In pyronone, two 1,3-hydrogen shift reaction paths are possible. Path I leads to the formation of 4-hydroxy-α-pyrone and Path II gives 2-hydroxy-γ-pyrone. Diketo form is found to be the most stable form followed by 4- hydroxy-α-pyrone and 2- hydroxy-γ-pyrone. Activation energy for Path I is lower than that fur Path II. Both the reactions are predicted to be endothermic. Inclusion of electron correlation lowers the energy barrierr and makes the reaction less endothermic. Variation of descriptors like chemical hardness and electrophilicity along the two different pathways has also been investigated. Effect of solvent on barrier heights has also been examined. Effect of different substituents (fluoro, methyl and phenyl) at position 6 of pyronone has also been studied.
Page(s): 887-890
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections: IJC-A Vol.45A(04) [April 2006]

Files in This Item:
File Description SizeFormat 
IJCA 45A(4) 887-890.pdf765.26 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.