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dc.contributor.author남원우*
dc.contributor.author조재흥*
dc.date.accessioned2016-08-28T12:08:35Z-
dc.date.available2016-08-28T12:08:35Z-
dc.date.issued2011*
dc.identifier.issn1523-7060*
dc.identifier.otherOAK-8224*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/222152-
dc.description.abstractHighly conjugated azines were prepared by solid state grinding of solid hydrazine and carbonyl compounds such as aldehydes and ketones, using a mortar and a pestle. Complete conversion to the azine product is generally achieved at room temperature within 24 h, without using solvents or additives. The solid-state reactions afford azines as the sole products with greater than 97% yield, producing only water and carbon dioxide as waste. © 2011 American Chemical Society.*
dc.languageEnglish*
dc.titleSynthesis of azines in solid state: Reactivity of solid hydrazine with aldehydes and ketones*
dc.typeArticle*
dc.relation.issue24*
dc.relation.volume13*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage6386*
dc.relation.lastpage6389*
dc.relation.journaltitleOrganic Letters*
dc.identifier.doi10.1021/ol202593g*
dc.identifier.wosidWOS:000297717800015*
dc.identifier.scopusid2-s2.0-84055224047*
dc.author.googleLee B.*
dc.author.googleHyung Lee K.*
dc.author.googleCho J.*
dc.author.googleNam W.*
dc.author.googleHur N.H.*
dc.contributor.scopusid남원우(7006569723)*
dc.contributor.scopusid조재흥(7403536408)*
dc.date.modifydate20240116111857*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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