Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation
العنوان: | Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation |
---|---|
المؤلفون: | Guoling Huang, Jian Li, Xiuwen Chen, Qiang Liu, Yubing Huang, Lu Chen, Yibiao Li, Xiaoliang Ji |
المصدر: | Chemical communications (Cambridge, England). 56(43) |
سنة النشر: | 2020 |
مصطلحات موضوعية: | Annulation, Chemistry, Metals and Alloys, chemistry.chemical_element, General Chemistry, Medicinal chemistry, Sulfur, Catalysis, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, chemistry.chemical_compound, Cascade, Potassium ethyl xanthate, Materials Chemistry, Ceramics and Composites |
الوصف: | The use of potassium ethyl xanthate (EtOCS2k) as a sulfur atom donor enabled the transition-metal-free [3 + 1 + 1] cascade annulation of isopropene derivatives with NH4I in DMSO/H2O, affording various 4-substituted isothiazoles in moderate to good yields with good functional group compatibility. Furthermore, Pd and Ag-catalyzed C5–H-selective direct oxidation dimerization of 4-substituted isothiazoles afforded 5,5′-bisisothiazoles. This series of reactions included the formation of new C–S, C–N, N–S, and C–C bonds via cascade addition, annulation, and direct C–H activation under mild conditions. |
تدمد: | 1364-548X |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4912de6868c259b4bd3e791fe01a61df https://pubmed.ncbi.nlm.nih.gov/32319987 |
Rights: | CLOSED |
رقم الانضمام: | edsair.doi.dedup.....4912de6868c259b4bd3e791fe01a61df |
قاعدة البيانات: | OpenAIRE |
ResultId |
1 |
---|---|
Header |
edsair OpenAIRE edsair.doi.dedup.....4912de6868c259b4bd3e791fe01a61df 845 3 unknown 844.6591796875 |
PLink |
https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....4912de6868c259b4bd3e791fe01a61df&custid=s6537998&authtype=sso |
FullText |
Array
(
[Availability] => 0
)
Array ( [0] => Array ( [Url] => https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4912de6868c259b4bd3e791fe01a61df# [Name] => EDS - OpenAIRE [Category] => fullText [Text] => View record in OpenAIRE [MouseOverText] => View record in OpenAIRE ) ) |
Items |
Array
(
[Name] => Title
[Label] => Title
[Group] => Ti
[Data] => Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation
)
Array ( [Name] => Author [Label] => Authors [Group] => Au [Data] => <searchLink fieldCode="AR" term="%22Guoling+Huang%22">Guoling Huang</searchLink><br /><searchLink fieldCode="AR" term="%22Jian+Li%22">Jian Li</searchLink><br /><searchLink fieldCode="AR" term="%22Xiuwen+Chen%22">Xiuwen Chen</searchLink><br /><searchLink fieldCode="AR" term="%22Qiang+Liu%22">Qiang Liu</searchLink><br /><searchLink fieldCode="AR" term="%22Yubing+Huang%22">Yubing Huang</searchLink><br /><searchLink fieldCode="AR" term="%22Lu+Chen%22">Lu Chen</searchLink><br /><searchLink fieldCode="AR" term="%22Yibiao+Li%22">Yibiao Li</searchLink><br /><searchLink fieldCode="AR" term="%22Xiaoliang+Ji%22">Xiaoliang Ji</searchLink> ) Array ( [Name] => TitleSource [Label] => Source [Group] => Src [Data] => <i>Chemical communications (Cambridge, England)</i>. 56(43) ) Array ( [Name] => DatePubCY [Label] => Publication Year [Group] => Date [Data] => 2020 ) Array ( [Name] => Subject [Label] => Subject Terms [Group] => Su [Data] => <searchLink fieldCode="DE" term="%22Annulation%22">Annulation</searchLink><br /><searchLink fieldCode="DE" term="%22Chemistry%22">Chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Metals+and+Alloys%22">Metals and Alloys</searchLink><br /><searchLink fieldCode="DE" term="%22chemistry%2Echemical%5Felement%22">chemistry.chemical_element</searchLink><br /><searchLink fieldCode="DE" term="%22General+Chemistry%22">General Chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Medicinal+chemistry%22">Medicinal chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Sulfur%22">Sulfur</searchLink><br /><searchLink fieldCode="DE" term="%22Catalysis%22">Catalysis</searchLink><br /><searchLink fieldCode="DE" term="%22Surfaces%2C+Coatings+and+Films%22">Surfaces, Coatings and Films</searchLink><br /><searchLink fieldCode="DE" term="%22Electronic%2C+Optical+and+Magnetic+Materials%22">Electronic, Optical and Magnetic Materials</searchLink><br /><searchLink fieldCode="DE" term="%22chemistry%2Echemical%5Fcompound%22">chemistry.chemical_compound</searchLink><br /><searchLink fieldCode="DE" term="%22Cascade%22">Cascade</searchLink><br /><searchLink fieldCode="DE" term="%22Potassium+ethyl+xanthate%22">Potassium ethyl xanthate</searchLink><br /><searchLink fieldCode="DE" term="%22Materials+Chemistry%22">Materials Chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Ceramics+and+Composites%22">Ceramics and Composites</searchLink> ) Array ( [Name] => Abstract [Label] => Description [Group] => Ab [Data] => The use of potassium ethyl xanthate (EtOCS2k) as a sulfur atom donor enabled the transition-metal-free [3 + 1 + 1] cascade annulation of isopropene derivatives with NH4I in DMSO/H2O, affording various 4-substituted isothiazoles in moderate to good yields with good functional group compatibility. Furthermore, Pd and Ag-catalyzed C5–H-selective direct oxidation dimerization of 4-substituted isothiazoles afforded 5,5′-bisisothiazoles. This series of reactions included the formation of new C–S, C–N, N–S, and C–C bonds via cascade addition, annulation, and direct C–H activation under mild conditions. ) Array ( [Name] => ISSN [Label] => ISSN [Group] => ISSN [Data] => 1364-548X ) Array ( [Name] => URL [Label] => Access URL [Group] => URL [Data] => <link linkTarget="URL" linkTerm="https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4912de6868c259b4bd3e791fe01a61df" linkWindow="_blank">https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4912de6868c259b4bd3e791fe01a61df</link><br /><link linkTarget="URL" linkTerm="https://pubmed.ncbi.nlm.nih.gov/32319987" linkWindow="_blank">https://pubmed.ncbi.nlm.nih.gov/32319987</link> ) Array ( [Name] => Copyright [Label] => Rights [Group] => Cpyrght [Data] => CLOSED ) Array ( [Name] => AN [Label] => Accession Number [Group] => ID [Data] => edsair.doi.dedup.....4912de6868c259b4bd3e791fe01a61df ) |
RecordInfo |
Array
(
[BibEntity] => Array
(
[Languages] => Array
(
[0] => Array
(
[Text] => Undetermined
)
)
[Subjects] => Array
(
[0] => Array
(
[SubjectFull] => Annulation
[Type] => general
)
[1] => Array
(
[SubjectFull] => Chemistry
[Type] => general
)
[2] => Array
(
[SubjectFull] => Metals and Alloys
[Type] => general
)
[3] => Array
(
[SubjectFull] => chemistry.chemical_element
[Type] => general
)
[4] => Array
(
[SubjectFull] => General Chemistry
[Type] => general
)
[5] => Array
(
[SubjectFull] => Medicinal chemistry
[Type] => general
)
[6] => Array
(
[SubjectFull] => Sulfur
[Type] => general
)
[7] => Array
(
[SubjectFull] => Catalysis
[Type] => general
)
[8] => Array
(
[SubjectFull] => Surfaces, Coatings and Films
[Type] => general
)
[9] => Array
(
[SubjectFull] => Electronic, Optical and Magnetic Materials
[Type] => general
)
[10] => Array
(
[SubjectFull] => chemistry.chemical_compound
[Type] => general
)
[11] => Array
(
[SubjectFull] => Cascade
[Type] => general
)
[12] => Array
(
[SubjectFull] => Potassium ethyl xanthate
[Type] => general
)
[13] => Array
(
[SubjectFull] => Materials Chemistry
[Type] => general
)
[14] => Array
(
[SubjectFull] => Ceramics and Composites
[Type] => general
)
)
[Titles] => Array
(
[0] => Array
(
[TitleFull] => Access to 4-substituted isothiazoles through three-component cascade annulation and their application in C-H activation
[Type] => main
)
)
)
[BibRelationships] => Array
(
[HasContributorRelationships] => Array
(
[0] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Guoling Huang
)
)
)
[1] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Jian Li
)
)
)
[2] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Xiuwen Chen
)
)
)
[3] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Qiang Liu
)
)
)
[4] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Yubing Huang
)
)
)
[5] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Lu Chen
)
)
)
[6] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Yibiao Li
)
)
)
[7] => Array
(
[PersonEntity] => Array
(
[Name] => Array
(
[NameFull] => Xiaoliang Ji
)
)
)
)
[IsPartOfRelationships] => Array
(
[0] => Array
(
[BibEntity] => Array
(
[Dates] => Array
(
[0] => Array
(
[D] => 23
[M] => 04
[Type] => published
[Y] => 2020
)
)
[Identifiers] => Array
(
[0] => Array
(
[Type] => issn-print
[Value] => 1364548X
)
[1] => Array
(
[Type] => issn-locals
[Value] => edsair
)
)
[Numbering] => Array
(
[0] => Array
(
[Type] => volume
[Value] => 56
)
[1] => Array
(
[Type] => issue
[Value] => 43
)
)
[Titles] => Array
(
[0] => Array
(
[TitleFull] => Chemical communications (Cambridge, England)
[Type] => main
)
)
)
)
)
)
)
|
IllustrationInfo |