Journalartikel

Synthesis of radialene-shaped pyrroles by multiple-anion-capture reactions of 1,3-dianions


AutorenlisteLanger, P; Döring, M; Schreiner, PR; Görls, H

Jahr der Veröffentlichung2001

Seiten2617-2627

ZeitschriftChemistry - A European Journal

Bandnummer7

Heftnummer12

ISSN0947-6539

VerlagWiley


Abstract
A now multicomponent reaction (multiple-anion-capture reaction) of 1,3-dianions with nitriles and oxalic acid-bis(imidoyl)chlorides is reported. This process allows for an efficient and regioselective synthesis of a variety of radialene-shaped pyrroles which constitute structurally new and interesting heterocyclic systems. The cyclization products can be considered as aza-analogues of the pharmacologically relevant substance class of 3-acetyltetramic acids. A rationalization of the experimental results is given based on quantum chemical computations.



Zitierstile

Harvard-ZitierstilLanger, P., Döring, M., Schreiner, P. and Görls, H. (2001) Synthesis of radialene-shaped pyrroles by multiple-anion-capture reactions of 1,3-dianions, Chemistry - A European Journal, 7(12), pp. 2617-2627. https://doi.org/10.1002/1521-3765(20010618)7:12<2617::AID-CHEM26170>3.0.CO;2-F

APA-ZitierstilLanger, P., Döring, M., Schreiner, P., & Görls, H. (2001). Synthesis of radialene-shaped pyrroles by multiple-anion-capture reactions of 1,3-dianions. Chemistry - A European Journal. 7(12), 2617-2627. https://doi.org/10.1002/1521-3765(20010618)7:12<2617::AID-CHEM26170>3.0.CO;2-F

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