Journal article
Synthetic access to 3,4-disubstituted pyroglutamates from tetramate derivatives from serine, allo-threonine and cysteine
- Abstract:
- A route allowing the conversion of substituted tetramates to 3,4-disubstituted pyroglutamates, making use of Suzuki coupling on an enol mesylate, followed by reduction, is both general and fully stereoselective.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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Access Document
- Files:
-
-
(Accepted manuscript, pdf, 978.9KB)
-
- Publisher copy:
- 10.1016/j.tet.2019.130561
Authors
Bibliographic Details
- Publisher:
- Elsevier Publisher's website
- Journal:
- Tetrahedron Journal website
- Volume:
- 75
- Issue:
- 40
- Article number:
- 130561
- Publication date:
- 2019-08-29
- Acceptance date:
- 2019-08-22
- DOI:
- ISSN:
-
0040-4020
Item Description
- Language:
- English
- Keywords:
- Pubs id:
-
pubs:1048447
- UUID:
-
uuid:1403e7ef-10cb-4cf3-ba64-7c93d34a2ce6
- Local pid:
- pubs:1048447
- Source identifiers:
-
1048447
- Deposit date:
- 2019-09-02
Terms of use
- Copyright holder:
- Elsevier Ltd.
- Copyright date:
- 2019
- Rights statement:
- © 2019 Elsevier Ltd. All rights reserved.
- Notes:
- This is the accepted manuscript version of the article. The final version is available online from Elsevier at: https://doi.org/10.1016/j.tet.2019.130561
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