<b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>

The synthesis of C7- to C16-alkyl maltosides in the presence of tin(IV) chloride as Lewis acid catalyst was performed. The characterization of the products and theoretical investigation of the crucial step in the synthesis were carried out. The preparation of the β-maltosides required reaction time...

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Main Authors: Zoran Marković, Jasmina Predojevic, Nedeljko T. Manojlovic
Format: Article
Language:English
Published: Chemical Society of Ethiopia 2011-04-01
Series:Bulletin of the Chemical Society of Ethiopia
Subjects:
PM3
Online Access:http://ajol.info/index.php/bcse/article/view/63368
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spelling doaj-7330977ea542479e80e0de1f1f7726502020-11-24T23:16:30ZengChemical Society of EthiopiaBulletin of the Chemical Society of Ethiopia1011-39241726-801X2011-04-012518390<b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>Zoran MarkovićJasmina PredojevicNedeljko T. ManojlovicThe synthesis of C7- to C16-alkyl maltosides in the presence of tin(IV) chloride as Lewis acid catalyst was performed. The characterization of the products and theoretical investigation of the crucial step in the synthesis were carried out. The preparation of the β-maltosides required reaction time of 1 h, and that of the α-maltosides was 72 h. The side products were the α-D-maltosidechloride and 2-hydroxy-β-maltoside, respectively. The PM3 calculation confirmed the formation of the kinetically controlled β-product.http://ajol.info/index.php/bcse/article/view/63368MaltoseSynthesis of maltosidesTin(IV) chloridePM3
collection DOAJ
language English
format Article
sources DOAJ
author Zoran Marković
Jasmina Predojevic
Nedeljko T. Manojlovic
spellingShingle Zoran Marković
Jasmina Predojevic
Nedeljko T. Manojlovic
<b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>
Bulletin of the Chemical Society of Ethiopia
Maltose
Synthesis of maltosides
Tin(IV) chloride
PM3
author_facet Zoran Marković
Jasmina Predojevic
Nedeljko T. Manojlovic
author_sort Zoran Marković
title <b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>
title_short <b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>
title_full <b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>
title_fullStr <b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>
title_full_unstemmed <b>Synthesis of C<sub>7</sub>-C<sub>16</sub>-alkyl maltosides in the presence of tin(IV) chloride as a Lewis acid catalyst</b>
title_sort <b>synthesis of c<sub>7</sub>-c<sub>16</sub>-alkyl maltosides in the presence of tin(iv) chloride as a lewis acid catalyst</b>
publisher Chemical Society of Ethiopia
series Bulletin of the Chemical Society of Ethiopia
issn 1011-3924
1726-801X
publishDate 2011-04-01
description The synthesis of C7- to C16-alkyl maltosides in the presence of tin(IV) chloride as Lewis acid catalyst was performed. The characterization of the products and theoretical investigation of the crucial step in the synthesis were carried out. The preparation of the β-maltosides required reaction time of 1 h, and that of the α-maltosides was 72 h. The side products were the α-D-maltosidechloride and 2-hydroxy-β-maltoside, respectively. The PM3 calculation confirmed the formation of the kinetically controlled β-product.
topic Maltose
Synthesis of maltosides
Tin(IV) chloride
PM3
url http://ajol.info/index.php/bcse/article/view/63368
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AT jasminapredojevic bsynthesisofcsub7subcsub16subalkylmaltosidesinthepresenceoftinivchlorideasalewisacidcatalystb
AT nedeljkotmanojlovic bsynthesisofcsub7subcsub16subalkylmaltosidesinthepresenceoftinivchlorideasalewisacidcatalystb
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