New synthesis of N-sulfinyl compound and its application for organic synthesisN-술피닐화합물의 새로운 합성 및 유기합성에서의 응용

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dc.contributor.advisorKim, Yong-Hae-
dc.contributor.advisor김용해-
dc.contributor.authorShin, Jai-Moo-
dc.contributor.author신재무-
dc.date.accessioned2011-12-13T04:24:28Z-
dc.date.available2011-12-13T04:24:28Z-
dc.date.issued1986-
dc.identifier.urihttp://library.kaist.ac.kr/search/detail/view.do?bibCtrlNo=60943&flag=dissertation-
dc.identifier.urihttp://hdl.handle.net/10203/31264-
dc.description학위논문(박사) - 한국과학기술원 : 화학과, 1986.2, [ viii, 81 p. ]-
dc.description.abstractN-Sulfinyl compounds have been widely studied and known to be very important heterocumulenes having a sulfur-centered structure of great synthetic utility. A new facile synthesis of N-sulfinyl compounds using N,N``-sulfinylbisimidazole(NSI) and N-(chlorosulfinyl) imidazole(NCI) was studied. Treatment of amine and its derivatives such as amines, amides, and sulfonamides with NSI and NCI, respectively, gives the corresponding N-sulfinyl compounds in quantitative yields under the mild conditions. NCI is a better reagent for the preparation of N-sulfinyl compounds. A new reaction of $\alpha$-hydroxy acids with N-sulfinylanilines has been studied. N-Sulfinylanilines react with $\alpha$-hydroxy acids to give $\alpha$-hydroxy anilides in quantitative yields under the mild conditions. The amidation reaction appears to involve intermolecular catalysis by the carboxyl group and intramolecular catalysis by the hydroxyl group.eng
dc.languageeng-
dc.publisher한국과학기술원-
dc.titleNew synthesis of N-sulfinyl compound and its application for organic synthesis-
dc.title.alternativeN-술피닐화합물의 새로운 합성 및 유기합성에서의 응용-
dc.typeThesis(Ph.D)-
dc.identifier.CNRN60943/325007-
dc.description.department한국과학기술원 : 화학과, -
dc.identifier.uid000815150-
dc.contributor.localauthorKim, Yong-Hae-
dc.contributor.localauthor김용해-
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