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A new synthesis of alihatic ketones from olefins via hydroboration under the influence of potassium t-butoxide and copper(I) iodide

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dc.contributor.author최정훈-
dc.date.accessioned2021-08-04T06:50:25Z-
dc.date.available2021-08-04T06:50:25Z-
dc.date.created2021-06-30-
dc.date.issued2003-10-16-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/76023-
dc.description.abstractThe alkyl groups of copper organoborate species which were syntheszed by the organoboranes originated from hydroboration of olefins, such as trialkylborane, B-hexyl-9-BBN, or B-hexyl-dicyclohexylborane, were transferred to aliphatic acyl halides under the influence of potassium t-butoxide and copper(I) iodide and THF-HMPA as a solvent.-
dc.publisher대한화학회-
dc.titleA new synthesis of alihatic ketones from olefins via hydroboration under the influence of potassium t-butoxide and copper(I) iodide-
dc.typeConference-
dc.contributor.affiliatedAuthor최정훈-
dc.identifier.bibliographicCitation대한화학회 추계 학술발표회-
dc.relation.isPartOf대한화학회 추계 학술발표회-
dc.citation.title대한화학회 추계 학술발표회-
dc.citation.conferencePlace부산 BEXCO-
dc.type.rimsCONF-
dc.description.journalClass2-
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