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|Title:||Stereocontrolled entry to the tricyclo[3.3.0]oxoheptane core of bielschowskysin by a [2+2] cycloaddition of an allene-butenolide||Authors:||Miao, R.
|Issue Date:||15-Apr-2009||Citation:||Miao, 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||Abstract:||As 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.||Source Title:||Tetrahedron Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/77052||ISSN:||00404039||DOI:||10.1016/j.tetlet.2009.01.131|
|Appears in Collections:||Staff Publications|
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