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<dublin_core schema="dc">
<dcvalue element="contributor" qualifier="author">Hur,&#x20;Joonseong</dcvalue>
<dcvalue element="contributor" qualifier="author">Jang,&#x20;Jaebong</dcvalue>
<dcvalue element="contributor" qualifier="author">Sim,&#x20;Jaehoon</dcvalue>
<dcvalue element="date" qualifier="accessioned">2024-01-19T15:04:37Z</dcvalue>
<dcvalue element="date" qualifier="available">2024-01-19T15:04:37Z</dcvalue>
<dcvalue element="date" qualifier="created">2022-01-25</dcvalue>
<dcvalue element="date" qualifier="issued">2021-03</dcvalue>
<dcvalue element="identifier" qualifier="issn">1661-6596</dcvalue>
<dcvalue element="identifier" qualifier="uri">https:&#x2F;&#x2F;pubs.kist.re.kr&#x2F;handle&#x2F;201004&#x2F;117284</dcvalue>
<dcvalue element="description" qualifier="abstract">gamma-Butyrolactone,&#x20;a&#x20;five-membered&#x20;lactone&#x20;moiety,&#x20;is&#x20;one&#x20;of&#x20;the&#x20;privileged&#x20;structures&#x20;of&#x20;diverse&#x20;natural&#x20;products&#x20;and&#x20;biologically&#x20;active&#x20;small&#x20;molecules.&#x20;Because&#x20;of&#x20;their&#x20;broad&#x20;spectrum&#x20;of&#x20;biological&#x20;and&#x20;pharmacological&#x20;activities,&#x20;synthetic&#x20;methods&#x20;for&#x20;gamma-butyrolactones&#x20;have&#x20;received&#x20;significant&#x20;attention&#x20;from&#x20;synthetic&#x20;and&#x20;medicinal&#x20;chemists&#x20;for&#x20;decades.&#x20;Recently,&#x20;new&#x20;developments&#x20;and&#x20;improvements&#x20;in&#x20;traditional&#x20;methods&#x20;have&#x20;been&#x20;reported&#x20;by&#x20;considering&#x20;synthetic&#x20;efficiency,&#x20;feasibility,&#x20;and&#x20;green&#x20;chemistry.&#x20;In&#x20;this&#x20;review,&#x20;the&#x20;pharmacological&#x20;activities&#x20;of&#x20;natural&#x20;and&#x20;synthetic&#x20;gamma-butyrolactones&#x20;are&#x20;described,&#x20;including&#x20;their&#x20;structures&#x20;and&#x20;bioassay&#x20;methods.&#x20;Mainly,&#x20;we&#x20;summarize&#x20;recent&#x20;advances,&#x20;occurring&#x20;during&#x20;the&#x20;past&#x20;decade,&#x20;in&#x20;the&#x20;construction&#x20;of&#x20;gamma-butyrolactone&#x20;classified&#x20;based&#x20;on&#x20;the&#x20;bond&#x20;formation&#x20;in&#x20;gamma-butyrolactone&#x20;between&#x20;(i)&#x20;C5-O1&#x20;bond,&#x20;(ii)&#x20;C4-C5&#x20;and&#x20;C2-O1&#x20;bonds,&#x20;(iii)&#x20;C3-C4&#x20;and&#x20;C2-O1&#x20;bonds,&#x20;(iv)&#x20;C3-C4&#x20;and&#x20;C5-O1&#x20;bonds,&#x20;(v)&#x20;C2-C3&#x20;and&#x20;C2-O1&#x20;bonds,&#x20;(vi)&#x20;C3-C4&#x20;bond,&#x20;and&#x20;(vii)&#x20;C2-O1&#x20;bond.&#x20;In&#x20;addition,&#x20;the&#x20;application&#x20;to&#x20;the&#x20;total&#x20;synthesis&#x20;of&#x20;natural&#x20;products&#x20;bearing&#x20;gamma-butyrolactone&#x20;scaffolds&#x20;is&#x20;described.</dcvalue>
<dcvalue element="language" qualifier="none">English</dcvalue>
<dcvalue element="publisher" qualifier="none">MDPI</dcvalue>
<dcvalue element="title" qualifier="none">A&#x20;Review&#x20;of&#x20;the&#x20;Pharmacological&#x20;Activities&#x20;and&#x20;Recent&#x20;Synthetic&#x20;Advances&#x20;of&#x20;gamma-Butyrolactones</dcvalue>
<dcvalue element="type" qualifier="none">Article</dcvalue>
<dcvalue element="identifier" qualifier="doi">10.3390&#x2F;ijms22052769</dcvalue>
<dcvalue element="description" qualifier="journalClass">1</dcvalue>
<dcvalue element="identifier" qualifier="bibliographicCitation">INTERNATIONAL&#x20;JOURNAL&#x20;OF&#x20;MOLECULAR&#x20;SCIENCES,&#x20;v.22,&#x20;no.5</dcvalue>
<dcvalue element="citation" qualifier="title">INTERNATIONAL&#x20;JOURNAL&#x20;OF&#x20;MOLECULAR&#x20;SCIENCES</dcvalue>
<dcvalue element="citation" qualifier="volume">22</dcvalue>
<dcvalue element="citation" qualifier="number">5</dcvalue>
<dcvalue element="description" qualifier="isOpenAccess">N</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scie</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scopus</dcvalue>
<dcvalue element="identifier" qualifier="wosid">000628287300001</dcvalue>
<dcvalue element="identifier" qualifier="scopusid">2-s2.0-85102103889</dcvalue>
<dcvalue element="relation" qualifier="journalWebOfScienceCategory">Biochemistry&#x20;&amp;&#x20;Molecular&#x20;Biology</dcvalue>
<dcvalue element="relation" qualifier="journalWebOfScienceCategory">Chemistry,&#x20;Multidisciplinary</dcvalue>
<dcvalue element="relation" qualifier="journalResearchArea">Biochemistry&#x20;&amp;&#x20;Molecular&#x20;Biology</dcvalue>
<dcvalue element="relation" qualifier="journalResearchArea">Chemistry</dcvalue>
<dcvalue element="type" qualifier="docType">Review</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">&amp;#947</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">-butyrolactone</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">pharmacological&#x20;activities</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">lactone&#x20;synthesis</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">lactonization</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">recent&#x20;advances</dcvalue>
</dublin_core>
