Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air
Experiments conducted with deuterated compounds demonstrated that during the reduction of S-alkylxanthates with triethylborane, the hydrogen atom transferred has several competing origins. Hydrogen abstraction from water (or an alcohol) is the most favourable route.
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2007-12-01
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Series: | Beilstein Journal of Organic Chemistry |
Online Access: | https://doi.org/10.1186/1860-5397-3-46 |
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doaj-be2d0b08603d44edb6334ace364f60682021-02-02T07:54:13ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972007-12-01314610.1186/1860-5397-3-461860-5397-3-46Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and airFlorent Allais0Jean Boivin1Van Tai Nguyen2Institut de Chimie des Substances Naturelles, C.N.R.S., Avenue de la Terrasse, 91198 Gif-sur-Yvette, FranceInstitut de Chimie des Substances Naturelles, C.N.R.S., Avenue de la Terrasse, 91198 Gif-sur-Yvette, FranceInstitut de Chimie des Substances Naturelles, C.N.R.S., Avenue de la Terrasse, 91198 Gif-sur-Yvette, FranceExperiments conducted with deuterated compounds demonstrated that during the reduction of S-alkylxanthates with triethylborane, the hydrogen atom transferred has several competing origins. Hydrogen abstraction from water (or an alcohol) is the most favourable route.https://doi.org/10.1186/1860-5397-3-46 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Florent Allais Jean Boivin Van Tai Nguyen |
spellingShingle |
Florent Allais Jean Boivin Van Tai Nguyen Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air Beilstein Journal of Organic Chemistry |
author_facet |
Florent Allais Jean Boivin Van Tai Nguyen |
author_sort |
Florent Allais |
title |
Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air |
title_short |
Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air |
title_full |
Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air |
title_fullStr |
Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air |
title_full_unstemmed |
Part 2. Mechanistic aspects of the reduction of S-alkyl-thionocarbonates in the presence of triethylborane and air |
title_sort |
part 2. mechanistic aspects of the reduction of s-alkyl-thionocarbonates in the presence of triethylborane and air |
publisher |
Beilstein-Institut |
series |
Beilstein Journal of Organic Chemistry |
issn |
1860-5397 |
publishDate |
2007-12-01 |
description |
Experiments conducted with deuterated compounds demonstrated that during the reduction of S-alkylxanthates with triethylborane, the hydrogen atom transferred has several competing origins. Hydrogen abstraction from water (or an alcohol) is the most favourable route. |
url |
https://doi.org/10.1186/1860-5397-3-46 |
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