A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide
A highly efficient and simple protocol for the synthesis of isothiocyanates and cyanamides from their respective amines in the presence of a mild, efficient, and non-toxic reagent tetrapropylammonium tribromide is described. High environmental acceptability of the reagents, cost effectiveness and hi...
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Slovenian Chemical Society
2017-12-01
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Online Access: | https://journals.matheo.si/index.php/ACSi/article/view/3342 |
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doaj-4a1e760290614b0986fadef5ca04bfb42020-11-25T00:50:00ZengSlovenian Chemical SocietyActa Chimica Slovenica1318-02071580-31552017-12-0164483284110.17344/acsi.2017.3342522A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromideUpasana Bora Sinha0Latonglila Jamir1Neivotsonuo Bernadette Kuotsu2Tovishe Phucho3Nagaland University Lumami-798627 Nagaland, IndiaDepartment of environmental sciences, Nagaland University, Lumami-798627, Nagaland, IndiaDepartment of Chemistry Kohima Science College (Autonomous) Kohima NagalandDepartment of Chemistry, Nagaland University, Lumami-798627, Nagaland, IndiaA highly efficient and simple protocol for the synthesis of isothiocyanates and cyanamides from their respective amines in the presence of a mild, efficient, and non-toxic reagent tetrapropylammonium tribromide is described. High environmental acceptability of the reagents, cost effectiveness and high yields are the important attributes of this methodology.https://journals.matheo.si/index.php/ACSi/article/view/3342TPATBdesulfurizationoxidationisothiocyanatessodium bicarbonatecyanamide |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Upasana Bora Sinha Latonglila Jamir Neivotsonuo Bernadette Kuotsu Tovishe Phucho |
spellingShingle |
Upasana Bora Sinha Latonglila Jamir Neivotsonuo Bernadette Kuotsu Tovishe Phucho A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide Acta Chimica Slovenica TPATB desulfurization oxidation isothiocyanates sodium bicarbonate cyanamide |
author_facet |
Upasana Bora Sinha Latonglila Jamir Neivotsonuo Bernadette Kuotsu Tovishe Phucho |
author_sort |
Upasana Bora Sinha |
title |
A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide |
title_short |
A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide |
title_full |
A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide |
title_fullStr |
A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide |
title_full_unstemmed |
A novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide |
title_sort |
novel one-pot synthesis of isothiocyanates and cyanamides from dithiocarbamate salts using environmentally benign reagent tetrapropylammonium tribromide |
publisher |
Slovenian Chemical Society |
series |
Acta Chimica Slovenica |
issn |
1318-0207 1580-3155 |
publishDate |
2017-12-01 |
description |
A highly efficient and simple protocol for the synthesis of isothiocyanates and cyanamides from their respective amines in the presence of a mild, efficient, and non-toxic reagent tetrapropylammonium tribromide is described. High environmental acceptability of the reagents, cost effectiveness and high yields are the important attributes of this methodology. |
topic |
TPATB desulfurization oxidation isothiocyanates sodium bicarbonate cyanamide |
url |
https://journals.matheo.si/index.php/ACSi/article/view/3342 |
work_keys_str_mv |
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