Spontaneous butenolide ring formation of pregnane-21-O-malonyl hemiesters under mild reaction conditions is facilitated by the 14β-hydroxy group present in all natural cardenolides

Maia de Pádua R, Meitinger N, Hennemann M, Schebitz P, Waibel R, Löber S, Gmeiner P, Clark T, Kreis W (2016)

Publication Language: English

Publication Type: Journal article, Original article

Publication year: 2016

Journal

Tetrahedron Elsevier

Publisher: Elsevier

Book Volume: 72

Pages Range: 4556-4563

DOI: 10.1016/j.tet.2016.06.024

Authors with CRIS profile

Nadine Meitinger Lehrstuhl für Pharmazeutische Biologie Matthias Hennemann Computer-Chemie-Centrum (CCC) Reiner Waibel Lehrstuhl für Pharmazeutische Chemie Stefan Löber Lehrstuhl für Pharmazeutische Chemie Peter Gmeiner Lehrstuhl für Pharmazeutische Chemie Timothy Clark Computer-Chemie-Centrum (CCC) Wolfgang Kreis Lehrstuhl für Pharmazeutische Biologie

Additional Organisation(s)

Emil-Fischer-Zentrum (Emil Fischer Center)

Related research project(s)

The genus Digitalis: Molecular taxonomy, preservation, active constituents and therapeutic applications (DIGITALIS) May 1, 2012 - April 30, 2016

How to cite

APA:

Maia de Pádua, R., Meitinger, N., Hennemann, M., Schebitz, P., Waibel, R., Löber, S.,... Kreis, W. (2016). Spontaneous butenolide ring formation of pregnane-21-O-malonyl hemiesters under mild reaction conditions is facilitated by the 14β-hydroxy group present in all natural cardenolides. Tetrahedron, 72, 4556-4563. https://doi.org/10.1016/j.tet.2016.06.024

MLA:

Maia de Pádua, Rodrigo, et al. "Spontaneous butenolide ring formation of pregnane-21-O-malonyl hemiesters under mild reaction conditions is facilitated by the 14β-hydroxy group present in all natural cardenolides." Tetrahedron 72 (2016): 4556-4563.

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