Intramolecular C-H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones
Intramolecular C-H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones
A new approach to the diastereoselective synthesis of thienofuranones is described in which an intramolecular 1,5-carbenoid C-H insertion adjacent to sulfur features as a key step.
metal carbene transformations, stereoselective-synthesis, organic-synthesis, cyclization, endo, exo-furofuranones
1772-1773
Skerry, Paul S.
c7ebeb7a-af57-4926-9ef6-6ff689c7077c
Swain, Nigel A.
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Harrowven, David C.
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Smyth, Donald
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Bruton, Gordon
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Brown, Richard C.D.
21ce697a-7c3a-480e-919f-429a3d8550f5
2004
Skerry, Paul S.
c7ebeb7a-af57-4926-9ef6-6ff689c7077c
Swain, Nigel A.
522cad04-7679-4f30-9b4a-c4351017edad
Harrowven, David C.
bddcfab6-dbde-49df-aec2-42abbcf5d10b
Smyth, Donald
f043ce2f-8793-4993-93ee-56545d7d06ff
Bruton, Gordon
aa387dc2-6884-402c-809a-5abf66ec4247
Brown, Richard C.D.
21ce697a-7c3a-480e-919f-429a3d8550f5
Skerry, Paul S., Swain, Nigel A., Harrowven, David C., Smyth, Donald, Bruton, Gordon and Brown, Richard C.D.
(2004)
Intramolecular C-H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones.
Chemical Communications, (15), .
(doi:10.1039/b402603a).
Abstract
A new approach to the diastereoselective synthesis of thienofuranones is described in which an intramolecular 1,5-carbenoid C-H insertion adjacent to sulfur features as a key step.
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Published date: 2004
Additional Information:
ChemComm
Keywords:
metal carbene transformations, stereoselective-synthesis, organic-synthesis, cyclization, endo, exo-furofuranones
Identifiers
Local EPrints ID: 20321
URI: http://eprints.soton.ac.uk/id/eprint/20321
ISSN: 1359-7345
PURE UUID: b9bbf92b-6125-407a-a599-80982909f86d
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Date deposited: 17 Feb 2006
Last modified: 16 Mar 2024 02:54
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Contributors
Author:
Paul S. Skerry
Author:
Nigel A. Swain
Author:
Donald Smyth
Author:
Gordon Bruton
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