Diastereoselective synthesis of 3,3-dimethylazetidines via an intramolecular iodine-mediated cyclization reaction

التفاصيل البيبلوغرافية
العنوان: Diastereoselective synthesis of 3,3-dimethylazetidines via an intramolecular iodine-mediated cyclization reaction
المؤلفون: Li-Ming Zhao, Wei Zhou, Hai-Shan Jin, Rui Sun
المصدر: RSC Advances. 6:15035-15038
بيانات النشر: Royal Society of Chemistry (RSC), 2016.
سنة النشر: 2016
مصطلحات موضوعية: 010405 organic chemistry, Chemistry, General Chemical Engineering, Bioactive molecules, Synthon, Intramolecular cyclization, chemistry.chemical_element, General Chemistry, 010402 general chemistry, Iodine, 01 natural sciences, 0104 chemical sciences, chemistry.chemical_compound, Intramolecular force, Moiety, Organic chemistry, Organic synthesis, Amine gas treating
الوصف: A number of bioactive molecules possess a 3,3-dimethylazetidine moiety. An iodine-mediated intramolecular cyclization reaction of γ-prenylated amines has been developed to provide a convenient route to 3,3-dimethylazetidines in a highly diastereoselective manner. The presented approach not only offers a new strategy for the synthesis of the bioactively important 3,3-dimethylazetidines but also provides an opportunity to extend the application of γ-prenylated amine synthons in organic synthesis.
تدمد: 2046-2069
DOI: 10.1039/c5ra21872a
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fdcde6b127224af89e4c358eda2af244
https://doi.org/10.1039/c5ra21872a
Rights: OPEN
رقم الانضمام: edsair.doi...........fdcde6b127224af89e4c358eda2af244
قاعدة البيانات: OpenAIRE
ResultId 1
Header edsair
OpenAIRE
edsair.doi...........fdcde6b127224af89e4c358eda2af244
815
3

unknown
815.477478027344
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi...........fdcde6b127224af89e4c358eda2af244&custid=s6537998&authtype=sso
FullText Array ( [Availability] => 0 )
Array ( [0] => Array ( [Url] => https://explore.openaire.eu/search/publication?articleId=doi_________::fdcde6b127224af89e4c358eda2af244# [Name] => EDS - OpenAIRE [Category] => fullText [Text] => View record in OpenAIRE [MouseOverText] => View record in OpenAIRE ) )
Items Array ( [Name] => Title [Label] => Title [Group] => Ti [Data] => Diastereoselective synthesis of 3,3-dimethylazetidines via an intramolecular iodine-mediated cyclization reaction )
Array ( [Name] => Author [Label] => Authors [Group] => Au [Data] => <searchLink fieldCode="AR" term="%22Li-Ming+Zhao%22">Li-Ming Zhao</searchLink><br /><searchLink fieldCode="AR" term="%22Wei+Zhou%22">Wei Zhou</searchLink><br /><searchLink fieldCode="AR" term="%22Hai-Shan+Jin%22">Hai-Shan Jin</searchLink><br /><searchLink fieldCode="AR" term="%22Rui+Sun%22">Rui Sun</searchLink> )
Array ( [Name] => TitleSource [Label] => Source [Group] => Src [Data] => <i>RSC Advances</i>. 6:15035-15038 )
Array ( [Name] => Publisher [Label] => Publisher Information [Group] => PubInfo [Data] => Royal Society of Chemistry (RSC), 2016. )
Array ( [Name] => DatePubCY [Label] => Publication Year [Group] => Date [Data] => 2016 )
Array ( [Name] => Subject [Label] => Subject Terms [Group] => Su [Data] => <searchLink fieldCode="DE" term="%22010405+organic+chemistry%22">010405 organic chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Chemistry%22">Chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22General+Chemical+Engineering%22">General Chemical Engineering</searchLink><br /><searchLink fieldCode="DE" term="%22Bioactive+molecules%22">Bioactive molecules</searchLink><br /><searchLink fieldCode="DE" term="%22Synthon%22">Synthon</searchLink><br /><searchLink fieldCode="DE" term="%22Intramolecular+cyclization%22">Intramolecular cyclization</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="%22010402+general+chemistry%22">010402 general chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Iodine%22">Iodine</searchLink><br /><searchLink fieldCode="DE" term="%2201+natural+sciences%22">01 natural sciences</searchLink><br /><searchLink fieldCode="DE" term="%220104+chemical+sciences%22">0104 chemical sciences</searchLink><br /><searchLink fieldCode="DE" term="%22chemistry%2Echemical%5Fcompound%22">chemistry.chemical_compound</searchLink><br /><searchLink fieldCode="DE" term="%22Intramolecular+force%22">Intramolecular force</searchLink><br /><searchLink fieldCode="DE" term="%22Moiety%22">Moiety</searchLink><br /><searchLink fieldCode="DE" term="%22Organic+chemistry%22">Organic chemistry</searchLink><br /><searchLink fieldCode="DE" term="%22Organic+synthesis%22">Organic synthesis</searchLink><br /><searchLink fieldCode="DE" term="%22Amine+gas+treating%22">Amine gas treating</searchLink> )
Array ( [Name] => Abstract [Label] => Description [Group] => Ab [Data] => A number of bioactive molecules possess a 3,3-dimethylazetidine moiety. An iodine-mediated intramolecular cyclization reaction of γ-prenylated amines has been developed to provide a convenient route to 3,3-dimethylazetidines in a highly diastereoselective manner. The presented approach not only offers a new strategy for the synthesis of the bioactively important 3,3-dimethylazetidines but also provides an opportunity to extend the application of γ-prenylated amine synthons in organic synthesis. )
Array ( [Name] => ISSN [Label] => ISSN [Group] => ISSN [Data] => 2046-2069 )
Array ( [Name] => DOI [Label] => DOI [Group] => ID [Data] => 10.1039/c5ra21872a )
Array ( [Name] => URL [Label] => Access URL [Group] => URL [Data] => <link linkTarget="URL" linkTerm="https://explore.openaire.eu/search/publication?articleId=doi_________::fdcde6b127224af89e4c358eda2af244" linkWindow="_blank">https://explore.openaire.eu/search/publication?articleId=doi_________::fdcde6b127224af89e4c358eda2af244</link><br /><link linkTarget="URL" linkTerm="https://doi.org/10.1039/c5ra21872a" linkWindow="_blank">https://doi.org/10.1039/c5ra21872a</link> )
Array ( [Name] => Copyright [Label] => Rights [Group] => Cpyrght [Data] => OPEN )
Array ( [Name] => AN [Label] => Accession Number [Group] => ID [Data] => edsair.doi...........fdcde6b127224af89e4c358eda2af244 )
RecordInfo Array ( [BibEntity] => Array ( [Identifiers] => Array ( [0] => Array ( [Type] => doi [Value] => 10.1039/c5ra21872a ) ) [Languages] => Array ( [0] => Array ( [Text] => Undetermined ) ) [PhysicalDescription] => Array ( [Pagination] => Array ( [PageCount] => 4 [StartPage] => 15035 ) ) [Subjects] => Array ( [0] => Array ( [SubjectFull] => 010405 organic chemistry [Type] => general ) [1] => Array ( [SubjectFull] => Chemistry [Type] => general ) [2] => Array ( [SubjectFull] => General Chemical Engineering [Type] => general ) [3] => Array ( [SubjectFull] => Bioactive molecules [Type] => general ) [4] => Array ( [SubjectFull] => Synthon [Type] => general ) [5] => Array ( [SubjectFull] => Intramolecular cyclization [Type] => general ) [6] => Array ( [SubjectFull] => chemistry.chemical_element [Type] => general ) [7] => Array ( [SubjectFull] => General Chemistry [Type] => general ) [8] => Array ( [SubjectFull] => 010402 general chemistry [Type] => general ) [9] => Array ( [SubjectFull] => Iodine [Type] => general ) [10] => Array ( [SubjectFull] => 01 natural sciences [Type] => general ) [11] => Array ( [SubjectFull] => 0104 chemical sciences [Type] => general ) [12] => Array ( [SubjectFull] => chemistry.chemical_compound [Type] => general ) [13] => Array ( [SubjectFull] => Intramolecular force [Type] => general ) [14] => Array ( [SubjectFull] => Moiety [Type] => general ) [15] => Array ( [SubjectFull] => Organic chemistry [Type] => general ) [16] => Array ( [SubjectFull] => Organic synthesis [Type] => general ) [17] => Array ( [SubjectFull] => Amine gas treating [Type] => general ) ) [Titles] => Array ( [0] => Array ( [TitleFull] => Diastereoselective synthesis of 3,3-dimethylazetidines via an intramolecular iodine-mediated cyclization reaction [Type] => main ) ) ) [BibRelationships] => Array ( [HasContributorRelationships] => Array ( [0] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Li-Ming Zhao ) ) ) [1] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Wei Zhou ) ) ) [2] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Hai-Shan Jin ) ) ) [3] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Rui Sun ) ) ) ) [IsPartOfRelationships] => Array ( [0] => Array ( [BibEntity] => Array ( [Dates] => Array ( [0] => Array ( [D] => 01 [M] => 01 [Type] => published [Y] => 2016 ) ) [Identifiers] => Array ( [0] => Array ( [Type] => issn-print [Value] => 20462069 ) [1] => Array ( [Type] => issn-locals [Value] => edsair ) [2] => Array ( [Type] => issn-locals [Value] => edsairFT ) ) [Numbering] => Array ( [0] => Array ( [Type] => volume [Value] => 6 ) ) [Titles] => Array ( [0] => Array ( [TitleFull] => RSC Advances [Type] => main ) ) ) ) ) ) )
IllustrationInfo