Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/29254
Title: Unraveling the reaction mechanism, enantio and diastereoselectivities of selenium ylide promoted epoxidation
Authors: Jaccob, Madhavan
Sabapathi, Gopal
Sundar, J Vijaya
Kolandaivel, P
Subramanian, V
Venuvanalingam, Ponnambalam
Keywords: Theoretical chemistry;Density functional calculations;Selenium ylides;Epoxidation;Enantio;Stereoselectivity;Diastereoselectivity;Fukui functions
Issue Date: 8-Aug-2014
Abstract: The reaction between chiral selenium ylide and benzaldehyde leads to the formation of (2S,3S)-trans-epoxide with high enantio- and diastereoselectivity. Density functional theory and Hartree-Fock calculations using 6-31G(d) basis set have been performed to understand the reaction mechanism and factors associated with enantio- and diastereoselectivities. Conformation of chiral selenium ylide has been found to have a strong influence on the stability of the initial addition transition state between ylide and benzaldehyde. Calculated enantio- and diastereoselectivities from the energy differences between B3LYP/6-31G(d) addition TSs are in good agreement with the experimental data. The rate and diastereoselectivity are controlled by the cisoid-transoid rotational transition state. Analysis of transition state geometries clearly reveals that unfavorable eclipsing interaction between phenyl groups of the benzaldehyde and ylidic substituents mainly governs the energy differences between the enantio and diastereomeric transition states. The favourable reactivity is also explained through Fukui function calculations.
Page(s): 1001-1009
URI: http://hdl.handle.net/123456789/29254
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.53A(08-09) [August-September 2014]

Files in This Item:
File Description SizeFormat 
IJCA 53A(8-9) 1001-1009_Suppl Data.pdfSupplementary Data44.79 kBAdobe PDFView/Open
IJCA 53A(8-9) 1001-1009.pdfMain Article282.96 kBAdobe PDFView/Open


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