Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.tetlet.2009.01.131
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. 
Gramani, S.G.
Lear, M.J. 
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
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