Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2009.01.131
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dc.titleStereocontrolled entry to the tricyclo[3.3.0]oxoheptane core of bielschowskysin by a [2+2] cycloaddition of an allene-butenolide
dc.contributor.authorMiao, R.
dc.contributor.authorGramani, S.G.
dc.contributor.authorLear, M.J.
dc.date.accessioned2014-06-23T05:50:19Z
dc.date.available2014-06-23T05:50:19Z
dc.date.issued2009-04-15
dc.identifier.citationMiao, R., Gramani, S.G., Lear, M.J. (2009-04-15). Stereocontrolled entry to the tricyclo[3.3.0]oxoheptane core of bielschowskysin by a [2+2] cycloaddition of an allene-butenolide. Tetrahedron Letters 50 (15) : 1731-1733. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2009.01.131
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77052
dc.description.abstractAs part of ongoing transannulation studies, the practical synthesis of an allene-linked γ-butenolide from l-malic acid and its substrate-controlled [2+2] photocycloaddition to the tricyclic core of bielschowskysin (1) are described. © 2009 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tetlet.2009.01.131
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.tetlet.2009.01.131
dc.description.sourcetitleTetrahedron Letters
dc.description.volume50
dc.description.issue15
dc.description.page1731-1733
dc.description.codenTELEA
dc.identifier.isiut000264428300021
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