Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6639
Title: Synthesis of <i style="">N</i>-hydroxy-<i style="">r</i>-2,<i style="">c</i>-6-diphenylpiperidines using DMD and their stereochemical studies by NMR spectra and semiempirical MO calculations
Authors: Thenmozhiyal, J C
Venkatraj, M
Jeyaraman, R
Ponnuswamy, S
Keywords: Dimethyldioxirane
diphenylpiperidine
conformation
MO calculation
Issue Date: Aug-2006
Publisher: CSIR
Series/Report no.: Int. Cl.<sup>8</sup> C07D
Abstract: <i style="">r</i><b style="">-</b>2,<i style="">c</i>-6-Diphenylpiperidin-4-ones <b style="">2-6</b> and <i style="">r</i>-2,<i style="">c</i>-6-diphenylpiperidine <b style="">7</b> are treated with DMD and the reaction is found to yield only the corresponding <i style="">N</i>-hydroxy derivatives <b style="">8-13</b>. The preferred conformations of the <i style="">N</i>-hydroxy compounds <b style="">8-13 </b>are analysed using the NMR spectra and semiempirical molecular orbital calculations. The <i style="">N</i>-hydroxy derivatives <b style="">8-13 </b>are<b style=""> </b>found to prefer distorted chair conformations.
Description: 1887-1893
URI: http://hdl.handle.net/123456789/6639
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.45B(08) [August 2006]

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