@prefix dbo: . @prefix dbr: . dbr:Oppenauer_oxidation dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Collins_reagent dbo:wikiPageWikiLink dbr:Alcohol_oxidation . @prefix foaf: . @prefix wikipedia-en: . wikipedia-en:Alcohol_oxidation foaf:primaryTopic dbr:Alcohol_oxidation . dbr:Swern_oxidation dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Diol_oxidation dbo:wikiPageWikiLink dbr:Alcohol_oxidation ; dbo:wikiPageRedirects dbr:Alcohol_oxidation . dbr:Nicolaou_Taxol_total_synthesis dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:ADH7 dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Collins_oxidation dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Ketone dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Aldehyde dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Organic_redox_reaction dbo:wikiPageWikiLink dbr:Alcohol_oxidation . @prefix rdf: . @prefix yago: . dbr:Alcohol_oxidation rdf:type yago:WikicatOrganicReactions , yago:ChemicalReaction113447361 , yago:PhysicalEntity100001930 , yago:NaturalProcess113518963 , yago:ChemicalProcess113446390 , yago:Process100029677 , dbo:Disease . @prefix rdfs: . dbr:Alcohol_oxidation rdfs:label "Oxidaci\u00F3n de alcoholes"@es , "\u9187\u7684\u6C27\u5316\u53CD\u5E94"@zh , "Alcohol oxidation"@en , "Oxydation d'un alcool"@fr , "Oxida\u00E7\u00E3o de \u00E1lcool"@pt , "\u0623\u0643\u0633\u062F\u0629 \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A"@ar , "Oxidace alkohol\u016F"@cs ; rdfs:comment "\u0623\u0643\u0633\u062F\u0629 \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A (\u0628\u0627\u0644\u0625\u0646\u062C\u0644\u064A\u0632\u064A\u0629: Alcohol oxidation)\u200F \u0647\u0648 \u0645\u0646 \u0623\u0647\u0645 \u0627\u0644\u062A\u0641\u0627\u0639\u0644\u0627\u062A \u0641\u064A \u0627\u0644\u0643\u064A\u0645\u064A\u0627\u0621 \u0627\u0644\u0639\u0636\u0648\u064A\u0629. \u062D\u064A\u062B \u0623\u0646 \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A \u0627\u0644\u0623\u0648\u0644\u064A\u0629 \u064A\u0645\u0643\u0646 \u0623\u0646 \u062A\u062A\u0623\u0643\u0633\u062F \u0625\u0644\u0649 \u0645\u0631\u0643\u0628\u0627\u062A \u0627\u0644\u0623\u0644\u062F\u0647\u0627\u064A\u062F \u0623\u0648 \u0625\u0644\u0649 \u0627\u0644\u0623\u062D\u0645\u0627\u0636 \u0627\u0644\u0643\u0631\u0628\u0648\u0643\u0633\u064A\u0644\u064A\u0629\u060C \u0628\u064A\u0646\u0645\u0627 \u062A\u062A\u0623\u0643\u0633\u062F \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A \u0627\u0644\u062B\u0627\u0646\u0648\u064A\u0629 \u0625\u0644\u0649 \u0645\u0631\u0643\u0628\u0627\u062A \u0627\u0644\u0643\u064A\u062A\u0648\u0646. \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A \u0627\u0644\u062B\u0627\u0644\u062B\u064A\u0629 \u0644\u064A\u0633 \u0644\u062F\u064A\u0647\u0627 \u0627\u0644\u0642\u0627\u0628\u064A\u0644\u064A\u0629 \u0644\u0644\u062A\u0623\u0643\u0633\u062F. \u0625\u0646 \u062A\u0641\u0627\u0639\u0644 \u0623\u0643\u0633\u062F\u0629 \u0627\u0644\u0643\u062D\u0648\u0644 \u0627\u0644\u0623\u0648\u0644\u064A \u0625\u0644\u0649 \u062D\u0645\u0636 \u0627\u0644\u0643\u0631\u0628\u0648\u0643\u0633\u064A\u0644\u064A\u0629 \u064A\u062C\u0628 \u0623\u0646 \u062A\u0645\u0631 \u0628\u0645\u0631\u062D\u0644\u0629 \u0645\u0631\u0643\u0628 \u0627\u0644\u0623\u0644\u062F\u064A\u0647\u064A\u062F \u0627\u0644\u062E\u0627\u0635 \u0628\u0647 \u0627\u0644\u0630\u064A \u064A\u062A\u0645 \u062A\u062D\u0648\u064A\u0644\u0647 \u0625\u0644\u0649 \u0627\u0644\u0623\u0644\u062F\u064A\u0647\u064A\u062F \u0627\u0644\u0645\u0627\u0626\u064A \u0639\u0646 \u0637\u0631\u064A\u0642 \u0645\u0641\u0627\u0639\u0644\u062A\u0647 \u0645\u0639 \u0627\u0644\u0645\u0627\u0621. \u0648\u0645\u0646 \u0627\u0644\u0645\u0645\u0643\u0646 \u0623\u0646 \u062A\u062A\u0648\u0642\u0641 \u0623\u0643\u0633\u062F\u0629 \u0627\u0644\u0643\u062D\u0648\u0644 \u0627\u0644\u0623\u0648\u0644\u064A\u0629 \u0639\u0646\u062F \u0645\u0631\u062D\u0644\u0629 \u0627\u0644\u0623\u0644\u062F\u0647\u064A\u062F \u0639\u0646 \u0637\u0631\u064A\u0642 \u0625\u062C\u0631\u0627\u0621 \u0627\u0644\u062A\u0641\u0627\u0639\u0644 \u0628\u063A\u064A\u0627\u0628 \u0627\u0644\u0645\u0627\u0621 \u062D\u064A\u062B \u0644\u0627 \u064A\u062A\u0643\u0648\u0646 \u0627\u0644\u0623\u0644\u062F\u064A\u0647\u064A\u062F \u0627\u0644\u0645\u0627\u0626\u064A ."@ar , "Alcohol oxidation is a class of organic reactions in which the alcohol functional group is converted into another functional group (e.g., aldehyde, ketone, carboxylic acid) in which carbon carries a higher oxidation state."@en , "\u9187\u7684\u6C27\u5316\u53CD\u5E94\u662F\u4E00\u7C7B\u91CD\u8981\u7684\u6709\u673A\u53CD\u5E94\u3002\u5176\u4E2D\uFF0C \n* \u4E00\u7D1A\u9187\uFF08R-CH2-OH\uFF09\u53EF\u88AB\u6C27\u5316\u4E3A\u919B\uFF08R-CHO\uFF09\u6216\u7FA7\u9178\uFF08R-CO2H\uFF09\uFF1B \n* \u4E8C\u7D1A\u9187\uFF08R1R2CH-OH\uFF09\u901A\u5E38\u6700\u540E\u6C27\u5316\u4E3A\u916E\uFF08R1R2C=O\uFF09\u7684\u5F62\u5F0F\uFF0C\u56E0\u70BA\u916E\u7121\u6CD5\u9032\u4E00\u6B65\u6C27\u5316\u70BA\u7FA7\u9178\uFF1B \n* \u4E09\u7D1A\u9187\uFF08R1R2R3C-OH\uFF09\u5219\u901A\u5E38\u96BE\u4E8E\u53D1\u751F\u6C27\u5316\u53CD\u5E94\u3002 \u76F4\u63A5\u6C27\u5316\u4F2F\u9187\u81F3\u7FA7\u9178\u901A\u5E38\u8981\u7ECF\u8FC7\u76F8\u5E94\u7684\u919B\u7684\u9636\u6BB5\uFF0C\u4E5F\u5C31\u662F\u5728\u7EE7\u7EED\u6C27\u5316\u4E3A\u7FA7\u9178\u524D\uFF0C\u4E0E\u6C34\u5148\u53CD\u5E94\u5F62\u6210\u919B\u7684\u6C34\u5408\u7269\uFF08R-CH(OH)2\uFF09\u3002"@zh , "La oxidaci\u00F3n de alcoholes es una reacci\u00F3n org\u00E1nica importante. Los alcoholes primarios (R-CH2-OH) pueden ser oxidados a aldeh\u00EDdos (R-CHO) o \u00E1cidos carbox\u00EDlicos (R-COOH), mientras que la oxidaci\u00F3n de alcoholes secundarios (R1R2CH-OH), normalmente termina formando cetonas (R1R2C=O). Los alcoholes terciarios (R1R2R3C-OH) generan olefinas mediante su oxidaci\u00F3n.\u200B A menudo es posible interrumpir la oxidaci\u00F3n de un alcohol primario en el nivel de aldeh\u00EDdo mediante la realizaci\u00F3n de la reacci\u00F3n en ausencia de agua, de modo que no se puedan formar hidratos de cetonas."@es , "Il existe deux types d'oxydation d'un alcool. \n* oxydation compl\u00E8te; \n* oxydation m\u00E9nag\u00E9e. L'oxydation d'un alcool conduit \u00E0 des compos\u00E9s diff\u00E9rents suivant que l'on a affaire \u00E0 des d\u00E9riv\u00E9s primaires, secondaires ou tertiaires."@fr , "Oxidace alkohol\u016F jsou organick\u00E9 redoxn\u00ED reakce alkohol\u016F, kdy se alkoholov\u00E1 funk\u010Dn\u00ED skupina m\u011Bn\u00ED na jinou (aldehyd, keton, karboxylovou kyselinu) s atomem uhl\u00EDku ve vy\u0161\u0161\u00EDm oxida\u010Dn\u00EDm \u010D\u00EDsle. Od\u0161t\u011Bpen\u00ED ekvivalentu hydridu p\u0159em\u011Bn\u00ED prim\u00E1rn\u00ED alkohol na aldehyd a sekund\u00E1rn\u00ED na keton. Oxidace prim\u00E1rn\u00EDch alkohol\u016F na karboxylov\u00E9 kyseliny obvykle prob\u00EDhaj\u00ED p\u0159es odpov\u00EDdaj\u00EDc\u00ED aldehydy, kter\u00E9 se reakcemi s vodou p\u0159em\u011B\u0148uj\u00ED na gemin\u00E1ln\u00ED dioly, R-CH(OH)2. Oxidace prim\u00E1rn\u00EDch alkohol\u016F na aldehydy bez tvorby karboxylov\u00FDch kyselin tak lze dos\u00E1hnout nep\u0159\u00EDtomnost\u00ED vody, bez n\u00ED\u017E dal\u0161\u00ED oxidace neprob\u00EDh\u00E1."@cs , "A oxida\u00E7\u00E3o de \u00E1lcoois \u00E9 uma rea\u00E7\u00E3o org\u00E2nica em que a fun\u00E7\u00E3o \u00E1lcool \u00E9 transformada em fun\u00E7\u00F5es org\u00E2nicas em que o carbono aumenta o n\u00FAmero de oxida\u00E7\u00E3o. Os \u00E1lcoois prim\u00E1rios (R-CH2-OH) podem ser oxidados a alde\u00EDdos (R-CHO) ou \u00E1cidos carbox\u00EDlicos (R-CO2H), enquanto a oxida\u00E7\u00E3o de \u00E1lcoois secund\u00E1rios (R1R2CH-OH) normalmente forma cetonas (R1R2C=O ), e \u00E1lcoois terci\u00E1rios (R1R2R3C-OH) n\u00E3o sofrem oxida\u00E7\u00E3o."@pt ; foaf:depiction , , , . @prefix dcterms: . @prefix dbc: . dbr:Alcohol_oxidation dcterms:subject dbc:Organic_redox_reactions ; dbo:abstract "Il existe deux types d'oxydation d'un alcool. \n* oxydation compl\u00E8te; \n* oxydation m\u00E9nag\u00E9e. L'oxydation d'un alcool conduit \u00E0 des compos\u00E9s diff\u00E9rents suivant que l'on a affaire \u00E0 des d\u00E9riv\u00E9s primaires, secondaires ou tertiaires."@fr , "La oxidaci\u00F3n de alcoholes es una reacci\u00F3n org\u00E1nica importante. Los alcoholes primarios (R-CH2-OH) pueden ser oxidados a aldeh\u00EDdos (R-CHO) o \u00E1cidos carbox\u00EDlicos (R-COOH), mientras que la oxidaci\u00F3n de alcoholes secundarios (R1R2CH-OH), normalmente termina formando cetonas (R1R2C=O). Los alcoholes terciarios (R1R2R3C-OH) generan olefinas mediante su oxidaci\u00F3n.\u200B La oxidaci\u00F3n directa de los alcoholes primarios a \u00E1cidos carbox\u00EDlicos normalmente transcurre a trav\u00E9s del correspondiente aldeh\u00EDdo, que luego se transforma por reacci\u00F3n con agua en un hidrato de aldeh\u00EDdo (R-CH(OH)2), antes de que pueda ser oxidado a \u00E1cido carbox\u00EDlico. A menudo es posible interrumpir la oxidaci\u00F3n de un alcohol primario en el nivel de aldeh\u00EDdo mediante la realizaci\u00F3n de la reacci\u00F3n en ausencia de agua, de modo que no se puedan formar hidratos de cetonas."@es , "\u0623\u0643\u0633\u062F\u0629 \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A (\u0628\u0627\u0644\u0625\u0646\u062C\u0644\u064A\u0632\u064A\u0629: Alcohol oxidation)\u200F \u0647\u0648 \u0645\u0646 \u0623\u0647\u0645 \u0627\u0644\u062A\u0641\u0627\u0639\u0644\u0627\u062A \u0641\u064A \u0627\u0644\u0643\u064A\u0645\u064A\u0627\u0621 \u0627\u0644\u0639\u0636\u0648\u064A\u0629. \u062D\u064A\u062B \u0623\u0646 \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A \u0627\u0644\u0623\u0648\u0644\u064A\u0629 \u064A\u0645\u0643\u0646 \u0623\u0646 \u062A\u062A\u0623\u0643\u0633\u062F \u0625\u0644\u0649 \u0645\u0631\u0643\u0628\u0627\u062A \u0627\u0644\u0623\u0644\u062F\u0647\u0627\u064A\u062F \u0623\u0648 \u0625\u0644\u0649 \u0627\u0644\u0623\u062D\u0645\u0627\u0636 \u0627\u0644\u0643\u0631\u0628\u0648\u0643\u0633\u064A\u0644\u064A\u0629\u060C \u0628\u064A\u0646\u0645\u0627 \u062A\u062A\u0623\u0643\u0633\u062F \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A \u0627\u0644\u062B\u0627\u0646\u0648\u064A\u0629 \u0625\u0644\u0649 \u0645\u0631\u0643\u0628\u0627\u062A \u0627\u0644\u0643\u064A\u062A\u0648\u0646. \u0627\u0644\u0643\u062D\u0648\u0644\u0627\u062A \u0627\u0644\u062B\u0627\u0644\u062B\u064A\u0629 \u0644\u064A\u0633 \u0644\u062F\u064A\u0647\u0627 \u0627\u0644\u0642\u0627\u0628\u064A\u0644\u064A\u0629 \u0644\u0644\u062A\u0623\u0643\u0633\u062F. \u0625\u0646 \u062A\u0641\u0627\u0639\u0644 \u0623\u0643\u0633\u062F\u0629 \u0627\u0644\u0643\u062D\u0648\u0644 \u0627\u0644\u0623\u0648\u0644\u064A \u0625\u0644\u0649 \u062D\u0645\u0636 \u0627\u0644\u0643\u0631\u0628\u0648\u0643\u0633\u064A\u0644\u064A\u0629 \u064A\u062C\u0628 \u0623\u0646 \u062A\u0645\u0631 \u0628\u0645\u0631\u062D\u0644\u0629 \u0645\u0631\u0643\u0628 \u0627\u0644\u0623\u0644\u062F\u064A\u0647\u064A\u062F \u0627\u0644\u062E\u0627\u0635 \u0628\u0647 \u0627\u0644\u0630\u064A \u064A\u062A\u0645 \u062A\u062D\u0648\u064A\u0644\u0647 \u0625\u0644\u0649 \u0627\u0644\u0623\u0644\u062F\u064A\u0647\u064A\u062F \u0627\u0644\u0645\u0627\u0626\u064A \u0639\u0646 \u0637\u0631\u064A\u0642 \u0645\u0641\u0627\u0639\u0644\u062A\u0647 \u0645\u0639 \u0627\u0644\u0645\u0627\u0621. \u0648\u0645\u0646 \u0627\u0644\u0645\u0645\u0643\u0646 \u0623\u0646 \u062A\u062A\u0648\u0642\u0641 \u0623\u0643\u0633\u062F\u0629 \u0627\u0644\u0643\u062D\u0648\u0644 \u0627\u0644\u0623\u0648\u0644\u064A\u0629 \u0639\u0646\u062F \u0645\u0631\u062D\u0644\u0629 \u0627\u0644\u0623\u0644\u062F\u0647\u064A\u062F \u0639\u0646 \u0637\u0631\u064A\u0642 \u0625\u062C\u0631\u0627\u0621 \u0627\u0644\u062A\u0641\u0627\u0639\u0644 \u0628\u063A\u064A\u0627\u0628 \u0627\u0644\u0645\u0627\u0621 \u062D\u064A\u062B \u0644\u0627 \u064A\u062A\u0643\u0648\u0646 \u0627\u0644\u0623\u0644\u062F\u064A\u0647\u064A\u062F \u0627\u0644\u0645\u0627\u0626\u064A ."@ar , "Oxidace alkohol\u016F jsou organick\u00E9 redoxn\u00ED reakce alkohol\u016F, kdy se alkoholov\u00E1 funk\u010Dn\u00ED skupina m\u011Bn\u00ED na jinou (aldehyd, keton, karboxylovou kyselinu) s atomem uhl\u00EDku ve vy\u0161\u0161\u00EDm oxida\u010Dn\u00EDm \u010D\u00EDsle. Od\u0161t\u011Bpen\u00ED ekvivalentu hydridu p\u0159em\u011Bn\u00ED prim\u00E1rn\u00ED alkohol na aldehyd a sekund\u00E1rn\u00ED na keton. Oxidace prim\u00E1rn\u00EDch alkohol\u016F na karboxylov\u00E9 kyseliny obvykle prob\u00EDhaj\u00ED p\u0159es odpov\u00EDdaj\u00EDc\u00ED aldehydy, kter\u00E9 se reakcemi s vodou p\u0159em\u011B\u0148uj\u00ED na gemin\u00E1ln\u00ED dioly, R-CH(OH)2. Oxidace prim\u00E1rn\u00EDch alkohol\u016F na aldehydy bez tvorby karboxylov\u00FDch kyselin tak lze dos\u00E1hnout nep\u0159\u00EDtomnost\u00ED vody, bez n\u00ED\u017E dal\u0161\u00ED oxidace neprob\u00EDh\u00E1."@cs , "\u9187\u7684\u6C27\u5316\u53CD\u5E94\u662F\u4E00\u7C7B\u91CD\u8981\u7684\u6709\u673A\u53CD\u5E94\u3002\u5176\u4E2D\uFF0C \n* \u4E00\u7D1A\u9187\uFF08R-CH2-OH\uFF09\u53EF\u88AB\u6C27\u5316\u4E3A\u919B\uFF08R-CHO\uFF09\u6216\u7FA7\u9178\uFF08R-CO2H\uFF09\uFF1B \n* \u4E8C\u7D1A\u9187\uFF08R1R2CH-OH\uFF09\u901A\u5E38\u6700\u540E\u6C27\u5316\u4E3A\u916E\uFF08R1R2C=O\uFF09\u7684\u5F62\u5F0F\uFF0C\u56E0\u70BA\u916E\u7121\u6CD5\u9032\u4E00\u6B65\u6C27\u5316\u70BA\u7FA7\u9178\uFF1B \n* \u4E09\u7D1A\u9187\uFF08R1R2R3C-OH\uFF09\u5219\u901A\u5E38\u96BE\u4E8E\u53D1\u751F\u6C27\u5316\u53CD\u5E94\u3002 \u76F4\u63A5\u6C27\u5316\u4F2F\u9187\u81F3\u7FA7\u9178\u901A\u5E38\u8981\u7ECF\u8FC7\u76F8\u5E94\u7684\u919B\u7684\u9636\u6BB5\uFF0C\u4E5F\u5C31\u662F\u5728\u7EE7\u7EED\u6C27\u5316\u4E3A\u7FA7\u9178\u524D\uFF0C\u4E0E\u6C34\u5148\u53CD\u5E94\u5F62\u6210\u919B\u7684\u6C34\u5408\u7269\uFF08R-CH(OH)2\uFF09\u3002"@zh , "A oxida\u00E7\u00E3o de \u00E1lcoois \u00E9 uma rea\u00E7\u00E3o org\u00E2nica em que a fun\u00E7\u00E3o \u00E1lcool \u00E9 transformada em fun\u00E7\u00F5es org\u00E2nicas em que o carbono aumenta o n\u00FAmero de oxida\u00E7\u00E3o. Os \u00E1lcoois prim\u00E1rios (R-CH2-OH) podem ser oxidados a alde\u00EDdos (R-CHO) ou \u00E1cidos carbox\u00EDlicos (R-CO2H), enquanto a oxida\u00E7\u00E3o de \u00E1lcoois secund\u00E1rios (R1R2CH-OH) normalmente forma cetonas (R1R2C=O ), e \u00E1lcoois terci\u00E1rios (R1R2R3C-OH) n\u00E3o sofrem oxida\u00E7\u00E3o. A oxida\u00E7\u00E3o indireta de \u00E1lcoois prim\u00E1rios em \u00E1cidos carbox\u00EDlicos ocorre normalmente atrav\u00E9s do alde\u00EDdo correspondente, que \u00E9 transformado atrav\u00E9s de um hidrato de alde\u00EDdo (R-CH(OH)2) por rea\u00E7\u00E3o com \u00E1gua. A oxida\u00E7\u00E3o de um \u00E1lcool prim\u00E1rio no n\u00EDvel de alde\u00EDdo \u00E9 poss\u00EDvel executando a rea\u00E7\u00E3o na aus\u00EAncia de \u00E1gua, de modo que nenhum hidrato de alde\u00EDdo possa ser formado."@pt , "Alcohol oxidation is a class of organic reactions in which the alcohol functional group is converted into another functional group (e.g., aldehyde, ketone, carboxylic acid) in which carbon carries a higher oxidation state. Through a variety of mechanisms, the removal of a hydride equivalent converts a primary or secondary alcohol to an aldehyde or ketone, respectively. The oxidation of primary alcohols to carboxylic acids normally proceeds via the corresponding aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH)2) by reaction with water. Thus, the oxidation of a primary alcohol at the aldehyde level without further oxidation to the carboxylic acid is possible by performing the reaction in absence of water, so that no aldehyde hydrate can be formed."@en ; dbo:wikiPageWikiLink dbr:Dimethyl_sulfoxide , dbr:Aluminium_isopropoxide , dbr:Carbonyl , dbr:Swern_oxidation , dbr:Pyridinium_dichromate , dbr:Oppenauer_oxidation , dbc:Organic_redox_reactions , dbr:Collins_reagent , dbr:Ruthenium_tetroxide , dbr:Organic_reaction , , dbr:Sulfonium-based_oxidation_of_alcohols_to_aldehydes , , dbr:Aldehyde , dbr:Pfitzner-Moffatt_oxidation , dbr:Jones_oxidation , dbr:Bleach , dbr:Carboxylic_acid , dbr:Parikh-Doering_oxidation , , dbr:TEMPO , dbr:Diol , , dbr:Pyridinium_chlorochromate , dbr:Ketone , dbr:Carbodiimide , , , dbr:Heyns_oxidation , dbr:Cyclohexanone , dbr:Lead_tetraacetate , , , dbr:Manganese_dioxide , dbr:Glycol_cleavage , dbr:Acetone , dbr:Sodium_hypochlorite , dbr:Dess-Martin_periodinane , dbr:Oxoammonium-catalyzed_oxidation , dbr:N-Methylmorpholine_N-oxide , dbr:Chromium_trioxide , dbr:Potassium_permanganate , , dbr:Oxidation_state , dbr:Electrophile , dbr:Oxalyl_chloride , dbr:Tetrapropylammonium_perruthenate , dbr:Ley_oxidation , dbr:NaOCl , dbr:Sodium_periodate . @prefix dbp: . @prefix dbt: . dbr:Alcohol_oxidation dbp:wikiPageUsesTemplate dbt:Organic_reactions , dbt:Main , dbt:Reflist , dbt:Alcohols , dbt:Wikiquote , dbt:Clear , dbt:Refimprove ; dbo:thumbnail ; dbo:wikiPageRevisionID 1100853278 . @prefix xsd: . dbr:Alcohol_oxidation dbo:wikiPageLength "5778"^^xsd:nonNegativeInteger ; dbo:wikiPageID 26517492 . @prefix owl: . dbr:Alcohol_oxidation owl:sameAs , , , , . @prefix yago-res: . dbr:Alcohol_oxidation owl:sameAs yago-res:Alcohol_oxidation , . @prefix wikidata: . dbr:Alcohol_oxidation owl:sameAs wikidata:Q3082836 , dbr:Alcohol_oxidation , , , . @prefix gold: . dbr:Alcohol_oxidation gold:hypernym dbr:Reaction . @prefix prov: . dbr:Alcohol_oxidation prov:wasDerivedFrom ; foaf:isPrimaryTopicOf wikipedia-en:Alcohol_oxidation . dbr:List_of_organic_reactions dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Stahl_oxidation dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Sulfonium-based_oxidation_of_alcohols_to_aldehydes dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Jim_Swan dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Pyridinium_chlorochromate dbo:wikiPageWikiLink dbr:Alcohol_oxidation . dbr:Oxidation_of_alcohols dbo:wikiPageWikiLink dbr:Alcohol_oxidation ; dbo:wikiPageRedirects dbr:Alcohol_oxidation .
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