at Google ScholarTitle data
Prause, Felix ; Kaldun, Johannes ; Arensmeyer, Benjamin ; Wennemann, Benedikt ; Fröhlich, Benjamin ; Scharnagel, Dagmar ; Breuning, Matthias:
Flexible and Modular Syntheses of Enantiopure 5-cis-Substituted Prolinamines from l-Pyroglutamic Acid.
In: Synthesis.
Vol. 47
(2015)
Issue 4
.
- pp. 575-586.
ISSN 0039-7881
DOI: https://doi.org/10.1055/s-0034-1379457
Abstract in another language
A wide range (25 examples) of 5-cis-substituted prolinamines is prepared in five to ten steps starting from cheap l-pyroglutamic acid. Three routes, differing mainly in the order of introduction of the substituents at the 5-cis position, the pyrrolidine nitrogen atom, and the exocyclic amino function, are successfully developed.
Further data
| Item Type: | Article in a journal |
|---|---|
| Refereed: | Yes |
| Keywords: | amines; ligands; stereoselective synthesis; pyrrolidines; prolinamines |
| Institutions of the University: | Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Professor Organic Chemistry > Professor Organic Chemistry - Univ.-Prof. Dr. Matthias Breuning Faculties Faculties > Faculty of Biology, Chemistry and Earth Sciences Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Professor Organic Chemistry |
| Result of work at the UBT: | Yes |
| DDC Subjects: | 500 Science > 540 Chemistry |
| Date Deposited: | 11 Jan 2022 13:00 |
| Last Modified: | 11 Jan 2022 13:00 |
| URI: | https://eref.uni-bayreuth.de/id/eprint/68302 |