An enantiocontrolled synthesis of a key intermediate to (+)-lactacystin
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kang, SungHo | ko |
| dc.contributor.author | Jun, HS | ko |
| dc.date.accessioned | 2013-03-02T20:17:45Z | - |
| dc.date.available | 2013-03-02T20:17:45Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1998-09 | - |
| dc.identifier.citation | CHEMICAL COMMUNICATIONS, no.18, pp.1929 - 1930 | - |
| dc.identifier.issn | 1359-7345 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/75326 | - |
| dc.description.abstract | An asymmetric synthesis of a key intermediate 16 to (+)-lactacystin 1 has been established starting from epoxide 2 via intramolecular mercurioamidation of allylic trichloroacetimidate 4 and concomitant addition-reduction of ester 13 by Pr-i MgBr, in which reduction of the intermediate ketone proceeded with complete stereoselectivity. | - |
| dc.language | English | - |
| dc.publisher | ROYAL SOC CHEMISTRY | - |
| dc.subject | MICROBIAL METABOLITE | - |
| dc.subject | NEUROBLASTOMA-CELLS | - |
| dc.subject | LACTACYSTIN | - |
| dc.subject | DIFFERENTIATION | - |
| dc.subject | REDUCTION | - |
| dc.subject | KETONES | - |
| dc.title | An enantiocontrolled synthesis of a key intermediate to (+)-lactacystin | - |
| dc.type | Article | - |
| dc.identifier.wosid | 000076134900003 | - |
| dc.type.rims | ART | - |
| dc.citation.issue | 18 | - |
| dc.citation.beginningpage | 1929 | - |
| dc.citation.endingpage | 1930 | - |
| dc.citation.publicationname | CHEMICAL COMMUNICATIONS | - |
| dc.contributor.localauthor | Kang, SungHo | - |
| dc.contributor.nonIdAuthor | Jun, HS | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | MICROBIAL METABOLITE | - |
| dc.subject.keywordPlus | NEUROBLASTOMA-CELLS | - |
| dc.subject.keywordPlus | LACTACYSTIN | - |
| dc.subject.keywordPlus | DIFFERENTIATION | - |
| dc.subject.keywordPlus | REDUCTION | - |
| dc.subject.keywordPlus | KETONES | - |
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