Abstract
Treatment of N-acyl-aminoacid dimethylamides of type 8 with HCl in toluene leads to lactones of type 9 in good yields via the intermediate formation of 2-oxazolin-5-ones.
Obrecht, Daniel; Heimgartner, Heinz (1984). Eine neue Lactonsynthese via 2-Oxazolin-5-one als Zwischenprodukte. Tetrahedron Letters, 25(16):1717-1720.
Treatment of N-acyl-aminoacid dimethylamides of type 8 with HCl in toluene leads to lactones of type 9 in good yields via the intermediate formation of 2-oxazolin-5-ones.
Treatment of N-acyl-aminoacid dimethylamides of type 8 with HCl in toluene leads to lactones of type 9 in good yields via the intermediate formation of 2-oxazolin-5-ones.
Item Type: | Journal Article, refereed, original work |
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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: | 1984 |
Deposited On: | 02 Jul 2014 14:31 |
Last Modified: | 24 Jan 2022 04:21 |
Publisher: | Elsevier |
ISSN: | 0040-4039 |
Funders: | Schweizerischer Nationalfonds zur Förderung der wissenchaftlichen Forschung, F. Hoffmann-La Roche & Co. AG, Basel |
OA Status: | Closed |
Publisher DOI: | https://doi.org/10.1016/S0040-4039(01)81153-9 |
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