Double asymmetric iodoamination; Synthesis of C-2 symmetric and meso-amino alcohols
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kang, SungHo | ko |
| dc.contributor.author | Ryu, DH | ko |
| dc.date.accessioned | 2013-03-02T20:21:31Z | - |
| dc.date.available | 2013-03-02T20:21:31Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1996-02 | - |
| dc.identifier.citation | CHEMICAL COMMUNICATIONS, no.3, pp.355 - 356 | - |
| dc.identifier.issn | 1359-7345 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/75359 | - |
| dc.description.abstract | Alkenic diols 2 and 14 are iodocyclized providing dihydro-1,3-oxazine 3 and dihydrooxazole 15 in 90 and 93% de, respectively, which are precursors of various C-2 symmetric and meso-amino alcohols. | - |
| dc.language | English | - |
| dc.publisher | ROYAL SOC CHEMISTRY | - |
| dc.subject | HIV-1 PROTEASE INHIBITORS | - |
| dc.subject | STEREOCONTROLLED SYNTHESIS | - |
| dc.subject | CRYSTAL-STRUCTURE | - |
| dc.title | Double asymmetric iodoamination; Synthesis of C-2 symmetric and meso-amino alcohols | - |
| dc.type | Article | - |
| dc.identifier.wosid | A1996UG03800035 | - |
| dc.identifier.scopusid | 2-s2.0-0002369896 | - |
| dc.type.rims | ART | - |
| dc.citation.issue | 3 | - |
| dc.citation.beginningpage | 355 | - |
| dc.citation.endingpage | 356 | - |
| dc.citation.publicationname | CHEMICAL COMMUNICATIONS | - |
| dc.contributor.localauthor | Kang, SungHo | - |
| dc.contributor.nonIdAuthor | Ryu, DH | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | HIV-1 PROTEASE INHIBITORS | - |
| dc.subject.keywordPlus | STEREOCONTROLLED SYNTHESIS | - |
| dc.subject.keywordPlus | CRYSTAL-STRUCTURE | - |
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