On the highly stereoselective addition of lithio-acetylides to alpha-hydroxy-ketones
On the highly stereoselective addition of lithio-acetylides to alpha-hydroxy-ketones
Addition of 2 equiv of a lithio-acetylide to an unprotected ?-hydroxy ketone is extremely stereoselective in examples where the two ketone substituents are relatively large.
5-endo-dig cyclizations, beta-iodofurans
2240-2242
Dunford, D.
378dc511-3641-43a7-8a8d-449545c8c56d
Guyader, M.
c3a54c84-c54b-4399-8894-d72f2e51abd9
Jones, S.
43516f9c-c999-4c10-86b6-43992e4e7a29
Knight, D.W.
dbe05fb8-fea1-4e2e-8555-0c72c3f5bc65
Hursthouse, M.B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Coles, S.J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
31 March 2008
Dunford, D.
378dc511-3641-43a7-8a8d-449545c8c56d
Guyader, M.
c3a54c84-c54b-4399-8894-d72f2e51abd9
Jones, S.
43516f9c-c999-4c10-86b6-43992e4e7a29
Knight, D.W.
dbe05fb8-fea1-4e2e-8555-0c72c3f5bc65
Hursthouse, M.B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Coles, S.J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Dunford, D., Guyader, M., Jones, S., Knight, D.W., Hursthouse, M.B. and Coles, S.J.
(2008)
On the highly stereoselective addition of lithio-acetylides to alpha-hydroxy-ketones.
Tetrahedron Letters, 49 (14), .
(doi:10.1016/j.tetlet.2008.02.032).
Abstract
Addition of 2 equiv of a lithio-acetylide to an unprotected ?-hydroxy ketone is extremely stereoselective in examples where the two ketone substituents are relatively large.
This record has no associated files available for download.
More information
Published date: 31 March 2008
Keywords:
5-endo-dig cyclizations, beta-iodofurans
Identifiers
Local EPrints ID: 54445
URI: http://eprints.soton.ac.uk/id/eprint/54445
ISSN: 0040-4039
PURE UUID: dfbf8123-b902-44c2-a035-ae3b1a999b1e
Catalogue record
Date deposited: 05 Aug 2008
Last modified: 16 Mar 2024 03:05
Export record
Altmetrics
Contributors
Author:
D. Dunford
Author:
M. Guyader
Author:
S. Jones
Author:
D.W. Knight
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics