Abstract
The cyclization reaction of the dimethylamides 2b, 5, 6 and 7, resulting from the reaction of mandelic acid with the aminoazirine 1, yields the 6-, 9-, 12- and 15-membered cyclic depsipeptides 10 - 13, respectively.
Obrecht, Daniel; Heimgartner, Heinz (1983). 3-dimethylamino-2,2-dimethyl-2h-azirin als aib-aequivalent bei heterocyclen-synthesen; synthese von 6-, 9-, 12- und 15-gliedrigen ringen. Tetrahedron Letters, 24(18):1921-1924.
Abstract
The cyclization reaction of the dimethylamides 2b, 5, 6 and 7, resulting from the reaction of mandelic acid with the aminoazirine 1, yields the 6-, 9-, 12- and 15-membered cyclic depsipeptides 10 - 13, respectively.
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Additional indexing
| Item Type: | Journal Article, refereed, original work |
|---|---|
| Communities & Collections: | 07 Faculty of Science > Department of Chemistry |
| Dewey Decimal Classification: | 540 Chemistry |
| Scopus Subject Areas: | Life Sciences > Biochemistry
Life Sciences > Drug Discovery Physical Sciences > Organic Chemistry |
| Language: | German |
| Date: | 1983 |
| Deposited On: | 09 Jul 2014 12:46 |
| Last Modified: | 24 Jan 2022 04:25 |
| Publisher: | Elsevier |
| ISSN: | 0040-4039 |
| Funders: | Schweizerischer Nationalfonds zur Förderung der wissenschaftlichen Forschung, F. Hoffmann-La Roche & Co. AG, Basel |
| OA Status: | Closed |
| Publisher DOI: | https://doi.org/10.1016/S0040-4039(00)81806-7 |
| Project Information: |
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Obrecht, Daniel