An Efficient Procedure For The Synthesis Of 2-n-boc-amino-3,5-diols

dc.creatorDias L.C.
dc.creatorFattori J.
dc.creatorPerez C.C.
dc.creatorde Oliveira V.M.
dc.creatorAguilar A.M.
dc.date2008
dc.date2015-06-30T19:24:16Z
dc.date2015-11-26T14:29:44Z
dc.date2015-06-30T19:24:16Z
dc.date2015-11-26T14:29:44Z
dc.date.accessioned2018-03-28T21:33:00Z
dc.date.available2018-03-28T21:33:00Z
dc.identifier
dc.identifierTetrahedron. , v. 64, n. 25, p. 5891 - 5903, 2008.
dc.identifier404020
dc.identifier10.1016/j.tet.2008.04.049
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-43449122151&partnerID=40&md5=b332a9d8d5f6676e6ea31b6b9df65cb5
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/106087
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/106087
dc.identifier2-s2.0-43449122151
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1246924
dc.descriptionWe wish to describe here the diastereoselective reaction between chiral N-Boc-α-amino aldehydes with both achiral allyltrichlorostannanes leading to 1,2-syn-N-Boc-α-amino alcohols, which are easily converted to the corresponding 4-N-Boc-amino-3-hydroxy ketones after treatment with catalytic amounts of OsO4 in the presence of NaIO4. After reduction of the carbonyl function, these 4-N-Boc-amino-3-hydroxy ketones were converted to 1-deoxy-5-hydroxy sphingosine analogues. © 2008 Elsevier Ltd. All rights reserved.
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dc.descriptionnote
dc.languageen
dc.publisher
dc.relationTetrahedron
dc.rightsfechado
dc.sourceScopus
dc.titleAn Efficient Procedure For The Synthesis Of 2-n-boc-amino-3,5-diols
dc.typeArtículos de revistas


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