Stereocontrolled entry to the tricyclo[3.3.0]oxoheptane core of bielschowskysin by a [2+2] cycloaddition of an allene-butenolide

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
Appears in Collections:	Staff Publications

There are no files associated with this item.

Check