DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kyu Tae Chang | - |
dc.contributor.author | Ki Chang Jang | - |
dc.contributor.author | Ho Yong Park | - |
dc.contributor.author | Young Kook Kim | - |
dc.contributor.author | Ki Hun Park | - |
dc.contributor.author | Woo Song Lee | - |
dc.date.accessioned | 2017-04-19T08:58:29Z | - |
dc.date.available | 2017-04-19T08:58:29Z | - |
dc.date.issued | 2001 | - |
dc.identifier.issn | 0385-5414 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/5617 | - |
dc.description.abstract | 3α-Acetoxy-4α-iodo-2α-(p-methoxybenzyl)pyrrolidine (2) and its enanti-omer (3) were synthesized via diastereoselective iodoamidation, starting from D- or L-tyrosine. The key step contains unfavorable 5-endo-trig cyclization and the diastereoselective addition of ethynylmagnesium bromide to aldehydes (9) by the chelation-controlled Cram cyclic model. | - |
dc.publisher | Elsevier | - |
dc.title | Diastereoselective Iodoamidation of 3-Acetoxybut-1-enylamines: synthesis of 3-acetoxy-4-iodo-2-(p-methoxy-benzyl)pyrolidines | - |
dc.title.alternative | Diastereoselective Iodoamidation of 3-Acetoxybut-1-enylamines: synthesis of 3-acetoxy-4-iodo-2-(p-methoxy-benzyl)pyrolidines | - |
dc.type | Article | - |
dc.citation.title | Heterocycles | - |
dc.citation.number | 6 | - |
dc.citation.endPage | 1179 | - |
dc.citation.startPage | 1173 | - |
dc.citation.volume | 55 | - |
dc.contributor.affiliatedAuthor | Kyu Tae Chang | - |
dc.contributor.affiliatedAuthor | Ho Yong Park | - |
dc.contributor.affiliatedAuthor | Young Kook Kim | - |
dc.contributor.affiliatedAuthor | Woo Song Lee | - |
dc.contributor.alternativeName | 장규태 | - |
dc.contributor.alternativeName | 장기창 | - |
dc.contributor.alternativeName | 박호용 | - |
dc.contributor.alternativeName | 김영국 | - |
dc.contributor.alternativeName | 박기훈 | - |
dc.contributor.alternativeName | 이우송 | - |
dc.identifier.bibliographicCitation | Heterocycles, vol. 55, no. 6, pp. 1173-1179 | - |
dc.identifier.doi | 10.3987/com-01-9206 | - |
dc.description.journalClass | Y | - |
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