Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9129
Title: CeCl<sub>3</sub>/Sm induced reductive cleavage of the S-S bond in disulfide: A novel method for the synthesis of <img src='/image/spc_char/beta.gif' border=0>-thioesters, thiol-esters and alkylphenyl sulfides
Authors: Li, Xue
Zhang, Songlin
Zhang, Yongmin
Keywords: CeCl<sub>3</sub>/Sm
<img src='/image/spc_char/beta.gif' border=0>-thioesters
thiol-esters
sulfides
Issue Date: Jul-2005
Publisher: CSIR
Series/Report no.: <b>Int</b>.<b>Cl</b>.<b><sup>7</sup> C 07 </b>
Abstract: Disulfide has been reduced by cerium trichloride and samarium in tetrahydrofuran to produce samarium thiolates. The “living” species reacts smoothly with <img src='/image/spc_char/alpha.gif' border=0> ,<img src='/image/spc_char/beta.gif' border=0>-unsaturated esters(nitriles) to afford <img src='/image/spc_char/beta.gif' border=0>-thioesters(nitrile) under mild and neutral conditions. The new thiolate anion also reacts with acyl halides, anhydrides and alkyl or benzyl halides to give thioesters and sulfides, respectively.
Description: 1527-1529
URI: http://hdl.handle.net/123456789/9129
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(07) [July 2005]

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