Journal article
Towards the total synthesis of keramaphidin B
- Abstract:
- The enantio- and diastereoselective Michael addition of a δ-valerolactone-derived pronucleophile to a substituted furanyl nitroolefin catalysed by a bifunctional cinchonine-derived thiourea has been used as the key stereocontrolling step in a new synthetic strategy to the heavily functionalised piperidine core of keramaphidin B.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Version of record, pdf, 233.8KB, Terms of use)
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- Publisher copy:
- 10.3762/bjoc.12.104
Authors
+ Engineering and Physical Sciences Research Council
More from this funder
- Funding agency for:
- Jakubec, P
- Farley, AJM
- Dixon, DJ
- Grant:
- Post-Doctoral Fellowship
- EP/M50659X/1
- Leadership Fellowship
- Publisher:
- Beilstein-Institut
- Journal:
- Beilstein Journal of Organic Chemistry More from this journal
- Volume:
- 12
- Pages:
- 1096-1100
- Publication date:
- 2016-05-30
- Acceptance date:
- 2016-05-10
- DOI:
- ISSN:
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1860-5397
- Pmid:
-
27340496
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:631390
- UUID:
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uuid:3272b95e-a1ad-42cf-9d25-71591191af52
- Local pid:
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pubs:631390
- Source identifiers:
-
631390
- Deposit date:
-
2016-09-06
Terms of use
- Copyright holder:
- Jakubec et al.
- Copyright date:
- 2016
- Rights statement:
- © 2016 Jakubec et al; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (http://www.beilstein-journals.org/bjoc)
- Licence:
- CC Attribution (CC BY)
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