2006
DOI: 10.1039/b602594c
|View full text |Cite
|
Sign up to set email alerts
|

Easy access to the family of thiazole N-oxides using HOF·CH3CN

Abstract: An efficient procedure for transferring an oxygen atom to thiazole-containing compounds, resulting in the corresponding N-oxides, was developed by using HOF x CH3CN; mild reaction conditions, high yields and easy purification are the main features of this novel route, while X-ray structural analysis reveals a hydrogen bond between the N-oxide functionality and a water molecule.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
6
0

Year Published

2006
2006
2022
2022

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 18 publications
(6 citation statements)
references
References 25 publications
0
6
0
Order By: Relevance
“…N -Oxidations, on the other hand, also systematically improve Δ E ST , but at the expense of an attractive T 1 energy. While these specific units have not been described in the literature, previously reported preparation of S -oxidized 22 and S , S -(di)oxidized 22,23 analogs of benzothiadiazole, as well as N -oxidized thiazoles, 24 bithiazoles, 25 and thiadiazoles 26 suggest that they are synthesizable.…”
mentioning
confidence: 99%
“…N -Oxidations, on the other hand, also systematically improve Δ E ST , but at the expense of an attractive T 1 energy. While these specific units have not been described in the literature, previously reported preparation of S -oxidized 22 and S , S -(di)oxidized 22,23 analogs of benzothiadiazole, as well as N -oxidized thiazoles, 24 bithiazoles, 25 and thiadiazoles 26 suggest that they are synthesizable.…”
mentioning
confidence: 99%
“…This has been demonstrated by the synthesis of a number of thiazole N-oxides using HOF Á MeCN. 17 One application of the more reactive halogens is in generating the highest known oxidation states of elements. A previous report that AuF 7 may be prepared by the reaction of AuF 5 with F 2 is not supported by calculations which clearly show that the reverse reaction is strongly exothermic with a low activation barrier.…”
Section: Halogensmentioning
confidence: 99%
“…These are found in a number of various food products and flavors and are used in the manufacturing of prepackaged food products including noodles [7]. Thiazoles help flavorists to create healthier crops by enhancing the flavor of meats and savory foods without the accumulation of excess salts or fats [8]. 1,2,4-Triazole derivatives and their bonded heterocyclic correspondents are well known for their different biological activities and 1,2,4-triazole rings have been combined into ligands used in coordination compounds.…”
Section: Introductionmentioning
confidence: 99%