Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9135
Title: A convenient synthesis of <img src='/image/spc_char/gamma.gif' border=0>-methyl <img src='/image/spc_char/alpha.gif' border=0> -(alkylidene)-<img src='/image/spc_char/gamma.gif' border=0>-butyrolactones
Authors: Shet, Jyoti B
Amonkar, Chandan P
Nadkarni, Vishnu S
Tilve, Santosh G
Issue Date: Jul-2005
Publisher: CSIR
Series/Report no.: <b style="">Int</b>.<b style="">Cl</b>.<b style=""><sup>7</sup> C 07 D 307/32</b>
Abstract: <img src='/image/spc_char/gamma.gif' border=0>-Methyl-<img src='/image/spc_char/alpha.gif' border=0> -(alkylidene substituted)-<img src='/image/spc_char/gamma.gif' border=0>-butyrolactones have been synthesized in two steps. The anion of allyl phos­phonate <b style="">1</b> is condensed with different carbonyl compounds to afford <img src='/image/spc_char/alpha.gif' border=0>,<img src='/image/spc_char/beta.gif' border=0>-unsaturated esters <b style="">2a-g</b>which are cyclised using 6<i style="">N</i> HCl to give title compounds.
Description: 1505-1508
URI: http://hdl.handle.net/123456789/9135
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(07) [July 2005]

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