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pro vyhledávání: '"tribromoisocyanuric acid"'
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Akademický článek
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Publikováno v:
Química Nova, Vol 36, Iss 2, Pp 320-323 (2013)
Primary, secondary and tertiary alcohols can be easily distinguished due to their reactivity towards tribromoisocyanuric acid (TBCA). The test is performed by adding TBCA to the alcohol in a test tube heated in a boiling water bath. Orange color deve
Externí odkaz:
https://doaj.org/article/b94fccc423ff4530b5ead7e8385f45e0
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:1403-1408
A simple method has been developed for homocoupling of terminal alkynes bearing different functional groups by reaction with CuI/tribromoisocyanuric acid/piperidine in acetonitrile at room temperature. A telescoped approach based on Hunsdiecker/Cadio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1929b9affaae2a369d8b3aadf806c12e
https://doi.org/10.1007/s00706-020-02673-8
https://doi.org/10.1007/s00706-020-02673-8
Publikováno v:
Letters in Organic Chemistry. 16:627-632
The co-halogenation reaction of alkynes with tri-bromoisocyanuric acid in acetic acid, followed by aqueous work-up produced α,α-di-bromoketones (44-84%), while the reaction in aqueous acetonitrile in the presence of KBr produced vicinal di-bromoalk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53e3852b64070be7e3dfc1b456721f27
https://doi.org/10.2174/1570178615666180803152951
https://doi.org/10.2174/1570178615666180803152951
Publikováno v:
Resources
Volume 10
Issue 2
Resources, Vol 10, Iss 17, p 17 (2021)
Volume 10
Issue 2
Resources, Vol 10, Iss 17, p 17 (2021)
Waste Electronic and Electrical Equipment (WEEE) is one of the fastest growing waste streams worldwide, with significant economic value due to the precious metals contained within. Currently, only a small share of the total globally produced quantity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::171abf509cea55a9393f018db0405467
Publikováno v:
Synthesis. 50:4867-4874
A simple and efficient one-pot protocol has been developed for the synthesis of thiazole derivatives from readily available starting materials. Tribromoisocyanuric acid was successfully used for α-monohalogenation of β-keto esters in aqueous medium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3009d2edb43c940f2cbf8aaf7cb15e86
https://doi.org/10.1055/s-0037-1610243
https://doi.org/10.1055/s-0037-1610243
A convenient Hofmann reaction of carboxamides and cyclic imides mediated by trihaloisocyanuric acids
Publikováno v:
Tetrahedron Letters. 83:153422
A simple, efficient and pot-economic approach in a single vessel has been developed for conversion of aromatic and aliphatic carboxamides into primary amines with one fewer carbom atom (Hofmann reaction) in 38–89 % yield by reacting with trichloro-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f7eee53d1c0cb31be42a19ef98344eb
https://doi.org/10.1016/j.tetlet.2021.153422
https://doi.org/10.1016/j.tetlet.2021.153422
Publikováno v:
Tetrahedron Letters. 61:152164
A simple and efficient one-pot protocol has been developed for the conversion of styrenes into 4-aryl-2-aminothiazoles using readily available starting materials. Tribromoisocyanuric acid was successfully used for the co-bromination and oxidation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6171310891ec8c67789dc99ee4340374
https://doi.org/10.1016/j.tetlet.2020.152164
https://doi.org/10.1016/j.tetlet.2020.152164
Publikováno v:
European Journal of Organic Chemistry. 2015:2733-2738
It is shown that both tribromoisocyanuric acid (TBCA) and trichloroisocyanuric acid (TCCA) are excellent reagents for direct halogenation of electron-rich aromatics under solvent-free, ball-milling conditions. The results are remarkable in light of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7485efb7d837fd4353eab9e3ed00e5bc
https://doi.org/10.1002/ejoc.201403463
https://doi.org/10.1002/ejoc.201403463