A short and efficient synthesis of (2S,3S,4S)-tert-butyl 3,4-dihydroxy-2-(methoxymethyl)-5-oxopyrrolidine-1-carboxylate

 |  Login

Show simple item record

dc.contributor Aalto-yliopisto fi
dc.contributor Aalto University en
dc.contributor.author Passiniemi, Mikko
dc.contributor.author Koskinen, Ari M.P.
dc.date.accessioned 2016-09-08T08:30:10Z
dc.date.issued 2010
dc.identifier.citation Passiniemi , M & Koskinen , A M P 2010 , ' A short and efficient synthesis of (2S,3S,4S)-tert-butyl 3,4-dihydroxy-2-(methoxymethyl)-5-oxopyrrolidine-1-carboxylate ' SYNTHESIS: STUTTGART , no. 16 , pp. 2816-2822 . en
dc.identifier.issn 0039-7881
dc.identifier.issn 1437-210X
dc.identifier.other PURE UUID: b9f79440-f57c-43c8-9b67-97c1d2f3bf9f
dc.identifier.other PURE ITEMURL: https://research.aalto.fi/en/publications/a-short-and-efficient-synthesis-of-2s3s4stertbutyl-34dihydroxy2methoxymethyl5oxopyrrolidine1carboxylate(b9f79440-f57c-43c8-9b67-97c1d2f3bf9f).html
dc.identifier.other PURE FILEURL: https://research.aalto.fi/files/7171211/ms156.pdf
dc.identifier.uri https://aaltodoc.aalto.fi/handle/123456789/21873
dc.description.abstract Asymmetric synthesis of the title compound was accomplished starting from L-serine. Stannoxane-mediated lactamization provided the key intermediate in good yield. en
dc.format.extent 2816-2822
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries SYNTHESIS: STUTTGART en
dc.relation.ispartofseries issue 16 en
dc.rights openAccess en
dc.subject.other 116 Chemical sciences en
dc.title A short and efficient synthesis of (2S,3S,4S)-tert-butyl 3,4-dihydroxy-2-(methoxymethyl)-5-oxopyrrolidine-1-carboxylate en
dc.type A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä fi
dc.description.version Peer reviewed en
dc.contributor.department School services, CHEM
dc.contributor.department Department of Chemistry en
dc.subject.keyword natural products
dc.subject.keyword stereoselective synthesis
dc.subject.keyword olefination
dc.subject.keyword alpha,beta-unsaturated lactam
dc.subject.keyword dihydroxylation
dc.subject.keyword 116 Chemical sciences
dc.identifier.urn URN:NBN:fi:aalto-201609083759
dc.identifier.doi 10.1055/s-0029-1218843
dc.type.version acceptedVersion


Files in this item

Files Size Format View

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record

Search archive


Advanced Search

article-iconSubmit a publication

Browse

My Account