A Corey-Seebach macrocyclisation strategy for the synthesis of riccardin C and an unnatural macrocyclic bis(bibenzyl) analogue
A Corey-Seebach macrocyclisation strategy for the synthesis of riccardin C and an unnatural macrocyclic bis(bibenzyl) analogue
A total synthesis of riccardin C has been accomplished using a Corey–Seebach reaction to effect macrocyclisation. The versatility of the strategy has also been demonstrated with a mimetic synthesis of an unnatural bis(bibenzyl) analogue.
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Almalki, Faisal
099cf883-b9f3-4a16-a4b2-38b272ed3ec4
Harrowven, David
bddcfab6-dbde-49df-aec2-42abbcf5d10b
Almalki, Faisal
099cf883-b9f3-4a16-a4b2-38b272ed3ec4
Harrowven, David
bddcfab6-dbde-49df-aec2-42abbcf5d10b
Almalki, Faisal and Harrowven, David
(2016)
A Corey-Seebach macrocyclisation strategy for the synthesis of riccardin C and an unnatural macrocyclic bis(bibenzyl) analogue.
European Journal of Organic Chemistry, .
(doi:10.1002/ejoc.201601179).
Abstract
A total synthesis of riccardin C has been accomplished using a Corey–Seebach reaction to effect macrocyclisation. The versatility of the strategy has also been demonstrated with a mimetic synthesis of an unnatural bis(bibenzyl) analogue.
Text
EJOC Corey Seebach Riccardin C.pdf
- Accepted Manuscript
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Accepted/In Press date: 20 September 2016
e-pub ahead of print date: 27 October 2016
Organisations:
Organic Chemistry: SCF
Identifiers
Local EPrints ID: 402164
URI: http://eprints.soton.ac.uk/id/eprint/402164
ISSN: 1434-193X
PURE UUID: 9a90a0e5-48a2-4b63-b276-41824f8dcfdd
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Date deposited: 02 Nov 2016 15:17
Last modified: 16 Mar 2024 02:46
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Author:
Faisal Almalki
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