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<dcvalue element="contributor" qualifier="author">Kang,&#x20;KH</dcvalue>
<dcvalue element="contributor" qualifier="author">Choi,&#x20;KI</dcvalue>
<dcvalue element="contributor" qualifier="author">Koh,&#x20;HY</dcvalue>
<dcvalue element="contributor" qualifier="author">Kim,&#x20;Y</dcvalue>
<dcvalue element="contributor" qualifier="author">Chung,&#x20;BY</dcvalue>
<dcvalue element="contributor" qualifier="author">Cho,&#x20;YS</dcvalue>
<dcvalue element="date" qualifier="accessioned">2024-01-21T12:04:37Z</dcvalue>
<dcvalue element="date" qualifier="available">2024-01-21T12:04:37Z</dcvalue>
<dcvalue element="date" qualifier="created">2021-09-05</dcvalue>
<dcvalue element="date" qualifier="issued">2001-08</dcvalue>
<dcvalue element="identifier" qualifier="issn">0039-7911</dcvalue>
<dcvalue element="identifier" qualifier="uri">https:&#x2F;&#x2F;pubs.kist.re.kr&#x2F;handle&#x2F;201004&#x2F;140285</dcvalue>
<dcvalue element="description" qualifier="abstract">Indium&#x20;mediated&#x20;allylation&#x20;of&#x20;nitro&#x20;group&#x20;was&#x20;first&#x20;achieved&#x20;with&#x20;four&#x20;allyl&#x20;bromides&#x20;in&#x20;aqueous&#x20;media.&#x20;Nitro-&#x20;benzenes&#x20;bearing&#x20;3-&#x20;and&#x2F;or&#x20;4-substituent(s)&#x20;gave&#x20;mainly&#x20;N,N-diallylated&#x20;(I&#x20;or&#x20;I&amp;apos;)&#x20;and&#x2F;or&#x20;N,O-diallylated&#x20;(II)&#x20;products&#x20;by&#x20;Method&#x20;A.&#x20;Allylation&#x20;of&#x20;nitrobenzenes&#x20;having&#x20;2-&#x20;(and&#x20;5-)&#x20;substituent(s)&#x20;could&#x20;be&#x20;achieved&#x20;only&#x20;with&#x20;crotyl&#x20;bromide&#x20;by&#x20;Method&#x20;B.</dcvalue>
<dcvalue element="language" qualifier="none">English</dcvalue>
<dcvalue element="publisher" qualifier="none">MARCEL&#x20;DEKKER&#x20;INC</dcvalue>
<dcvalue element="subject" qualifier="none">N-ARYLHYDROXYLAMINES</dcvalue>
<dcvalue element="subject" qualifier="none">CHLORIDE</dcvalue>
<dcvalue element="subject" qualifier="none">NITROARENES</dcvalue>
<dcvalue element="subject" qualifier="none">REDUCTION</dcvalue>
<dcvalue element="title" qualifier="none">Indium&#x20;mediated&#x20;allylation&#x20;of&#x20;nitro&#x20;group&#x20;on&#x20;nitrobenzene&#x20;derivatives&#x20;in&#x20;aqueous&#x20;media</dcvalue>
<dcvalue element="type" qualifier="none">Article</dcvalue>
<dcvalue element="identifier" qualifier="doi">10.1081&#x2F;SCC-100104827</dcvalue>
<dcvalue element="description" qualifier="journalClass">1</dcvalue>
<dcvalue element="identifier" qualifier="bibliographicCitation">SYNTHETIC&#x20;COMMUNICATIONS,&#x20;v.31,&#x20;no.15,&#x20;pp.2277&#x20;-&#x20;2286</dcvalue>
<dcvalue element="citation" qualifier="title">SYNTHETIC&#x20;COMMUNICATIONS</dcvalue>
<dcvalue element="citation" qualifier="volume">31</dcvalue>
<dcvalue element="citation" qualifier="number">15</dcvalue>
<dcvalue element="citation" qualifier="startPage">2277</dcvalue>
<dcvalue element="citation" qualifier="endPage">2286</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scie</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scopus</dcvalue>
<dcvalue element="identifier" qualifier="wosid">000170244600009</dcvalue>
<dcvalue element="identifier" qualifier="scopusid">2-s2.0-0034903609</dcvalue>
<dcvalue element="relation" qualifier="journalWebOfScienceCategory">Chemistry,&#x20;Organic</dcvalue>
<dcvalue element="relation" qualifier="journalResearchArea">Chemistry</dcvalue>
<dcvalue element="type" qualifier="docType">Article</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">N-ARYLHYDROXYLAMINES</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">CHLORIDE</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">NITROARENES</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">REDUCTION</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">indium</dcvalue>
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