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3-dimethylamino-2,2-dimethyl-2h-azirin als aib-aequivalent bei heterocyclen-synthesen; synthese von 6-, 9-, 12- und 15-gliedrigen ringen


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.

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
Language:German
Date:1983
Deposited On:09 Jul 2014 12:46
Last Modified:18 Apr 2018 11:45
Publisher:Elsevier
ISSN:0040-4039
Funders:Schweizerischer Nationalfonds zur Förderung der wissenschaftlichen Forschung, F. Hoffmann-La Roche & Co. AG, Basel
OA Status:Closed
Project Information:
  • : FunderSNSF
  • : Grant ID
  • : Project TitleSchweizerischer Nationalfonds zur Förderung der wissenschaftlichen Forschung
  • : Funder
  • : Grant ID
  • : Project TitleF. Hoffmann-La Roche & Co. AG, Basel

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