<?xml version="1.0" encoding="utf-8" standalone="no"?>
<dublin_core schema="dc">
<dcvalue element="contributor" qualifier="author">Song,&#x20;R</dcvalue>
<dcvalue element="contributor" qualifier="author">Kim,&#x20;KM</dcvalue>
<dcvalue element="contributor" qualifier="author">Lee,&#x20;SS</dcvalue>
<dcvalue element="contributor" qualifier="author">Sohn,&#x20;YS</dcvalue>
<dcvalue element="date" qualifier="accessioned">2024-01-21T13:38:22Z</dcvalue>
<dcvalue element="date" qualifier="available">2024-01-21T13:38:22Z</dcvalue>
<dcvalue element="date" qualifier="created">2022-01-10</dcvalue>
<dcvalue element="date" qualifier="issued">2000-08-07</dcvalue>
<dcvalue element="identifier" qualifier="issn">0020-1669</dcvalue>
<dcvalue element="identifier" qualifier="uri">https:&#x2F;&#x2F;pubs.kist.re.kr&#x2F;handle&#x2F;201004&#x2F;141169</dcvalue>
<dcvalue element="description" qualifier="abstract">A&#x20;novel&#x20;series&#x20;of&#x20;(diamine)platinum(IV)&#x20;complexes&#x20;of&#x20;mixed&#x20;carboxylates&#x20;have&#x20;been&#x20;synthesized&#x20;by&#x20;electrophilic&#x20;substitution&#x20;of&#x20;the&#x20;tetrahydroxoplatinum(IV)&#x20;complex&#x20;(dach)Pt(OH)(4)&#x20;(dach&#x20;=&#x20;trans-(+&#x2F;-)-1,2-diaminocyclohexane)&#x20;with&#x20;three&#x20;different&#x20;carboxylic&#x20;anhydrides,&#x20;pivalic,&#x20;acetic,&#x20;and&#x20;trifluoroacetic&#x20;anhydrides.&#x20;Consecutive&#x20;two-step&#x20;acylations&#x20;with&#x20;two&#x20;different&#x20;carboxylic&#x20;anhydrides&#x20;in&#x20;acetone&#x20;or&#x20;dichloromethane&#x20;gave&#x20;the&#x20;mixed&#x20;carboxylate&#x20;complexes&#x20;(dach)Pt(O2CR)(x)(O2CR&amp;apos;)(4-x)&#x20;(R&#x20;=&#x20;C(CH3)(3)&#x20;or&#x20;CF3,&#x20;R&#x20;=&#x20;CH3,&#x20;x&#x20;=&#x20;1-4)&#x20;including&#x20;all&#x20;the&#x20;possible&#x20;stereoisomers,&#x20;which&#x20;could&#x20;be&#x20;separated&#x20;and&#x20;identified&#x20;by&#x20;means&#x20;of&#x20;HPLC,&#x20;column&#x20;chromatography,&#x20;H-1&#x20;NMR,&#x20;and&#x20;X-ray&#x20;crystallography.&#x20;From&#x20;analysis&#x20;of&#x20;the&#x20;reaction&#x20;products&#x20;we&#x20;have&#x20;found&#x20;that&#x20;the&#x20;positions&#x20;of&#x20;electrophilic&#x20;substitution&#x20;of&#x20;(dach)Pt(OH)(4)&#x20;were&#x20;influenced&#x20;by&#x20;the&#x20;kinds&#x20;of&#x20;carboxylic&#x20;anhydrides&#x20;exhibiting&#x20;different&#x20;electrophilicity&#x20;or&#x20;steric&#x20;effects.&#x20;The&#x20;initial&#x20;substitution&#x20;by&#x20;the&#x20;first&#x20;reactant&#x20;occurs&#x20;more&#x20;favorably&#x20;on&#x20;axial&#x20;OH,&#x20;but&#x20;in&#x20;the&#x20;case&#x20;of&#x20;pivalic&#x20;anhydride,&#x20;equatorial&#x20;substitution&#x20;is&#x20;favored&#x20;probably&#x20;because&#x20;of&#x20;the&#x20;bulkiness&#x20;of&#x20;the&#x20;pivalate&#x20;group.&#x20;Such&#x20;a&#x20;result&#x20;seems&#x20;to&#x20;be&#x20;related&#x20;to&#x20;their&#x20;stereochemical&#x20;factors&#x20;rather&#x20;than&#x20;to&#x20;differences&#x20;in&#x20;electrophilicity.&#x20;The&#x20;lipophilicity&#x20;of&#x20;the&#x20;title&#x20;complexes&#x20;was&#x20;affected&#x20;not&#x20;only&#x20;by&#x20;the&#x20;carbon&#x20;numbers&#x20;of&#x20;substituents&#x20;but&#x20;also&#x20;by&#x20;the&#x20;conformation&#x20;of&#x20;the&#x20;resulting&#x20;compound.</dcvalue>
<dcvalue element="language" qualifier="none">English</dcvalue>
<dcvalue element="publisher" qualifier="none">AMER&#x20;CHEMICAL&#x20;SOC</dcvalue>
<dcvalue element="subject" qualifier="none">PLATINUM(IV)&#x20;COMPLEXES</dcvalue>
<dcvalue element="subject" qualifier="none">ANTICANCER&#x20;DRUG</dcvalue>
<dcvalue element="subject" qualifier="none">PHASE-I</dcvalue>
<dcvalue element="subject" qualifier="none">ANTITUMOR</dcvalue>
<dcvalue element="subject" qualifier="none">REDUCTION</dcvalue>
<dcvalue element="subject" qualifier="none">DNA</dcvalue>
<dcvalue element="title" qualifier="none">Electrophilic&#x20;substitution&#x20;of&#x20;(diamine)tetrahydroxoplatinum(IV)&#x20;with&#x20;carboxylic&#x20;anhydrides.&#x20;Synthesis&#x20;and&#x20;characterization&#x20;of&#x20;(diamine)platinum(IV)&#x20;complexes&#x20;of&#x20;mixed&#x20;carboxylates</dcvalue>
<dcvalue element="type" qualifier="none">Article</dcvalue>
<dcvalue element="identifier" qualifier="doi">10.1021&#x2F;ic9913886</dcvalue>
<dcvalue element="description" qualifier="journalClass">1</dcvalue>
<dcvalue element="identifier" qualifier="bibliographicCitation">INORGANIC&#x20;CHEMISTRY,&#x20;v.39,&#x20;no.16,&#x20;pp.3567&#x20;-&#x20;3571</dcvalue>
<dcvalue element="citation" qualifier="title">INORGANIC&#x20;CHEMISTRY</dcvalue>
<dcvalue element="citation" qualifier="volume">39</dcvalue>
<dcvalue element="citation" qualifier="number">16</dcvalue>
<dcvalue element="citation" qualifier="startPage">3567</dcvalue>
<dcvalue element="citation" qualifier="endPage">3571</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scie</dcvalue>
<dcvalue element="description" qualifier="journalRegisteredClass">scopus</dcvalue>
<dcvalue element="identifier" qualifier="wosid">000088717900021</dcvalue>
<dcvalue element="identifier" qualifier="scopusid">2-s2.0-0034617582</dcvalue>
<dcvalue element="relation" qualifier="journalWebOfScienceCategory">Chemistry,&#x20;Inorganic&#x20;&amp;&#x20;Nuclear</dcvalue>
<dcvalue element="relation" qualifier="journalResearchArea">Chemistry</dcvalue>
<dcvalue element="type" qualifier="docType">Article</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">PLATINUM(IV)&#x20;COMPLEXES</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">ANTICANCER&#x20;DRUG</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">PHASE-I</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">ANTITUMOR</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">REDUCTION</dcvalue>
<dcvalue element="subject" qualifier="keywordPlus">DNA</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">Platinum</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">Anticancer&#x20;drug</dcvalue>
<dcvalue element="subject" qualifier="keywordAuthor">Electrophilic&#x20;substitution</dcvalue>
</dublin_core>
