Volume 20, Issue 3‐4 p. 454-470
Regular Article/Special Issue Honoring Professor Nina Berova

Determination of the absolute configurations of natural products via density functional theory calculations of vibrational circular dichroism, electronic circular dichroism, and optical rotation: The iso‐schizozygane alkaloids isoschizogaline and isoschizogamine

Philip J. Stephens

Corresponding Author

Department of Chemistry, University of Southern California, Los Angeles, California

Department of Chemistry, University of Southern California, University Park Campus, Los Angeles, CA 90089‐0482Search for more papers by this author
Jian‐Jung Pan

Department of Chemistry, University of Southern California, Los Angeles, California

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Frank J. Devlin

Department of Chemistry, University of Southern California, Los Angeles, California

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Marie Urbanová

Department of Physics and Measurements, Institute of Chemical Technology, Prague, Technicka 5, Prague, Czech Republic

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Ondřej Julínek

Department of Analytical Chemistry, Institute of Chemical Technology, Prague, Technicka 5, Prague, Czech Republic

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Josef Hájíček

Synthesis Development Group II, R&D Division, Zentiva, a.s., U Kabelovny 130, Prague 10, Czech Republic

Department of Organic and Nuclear Chemistry, Faculty of Science, Charles University, Hlavova 8, Prague 2, Czech Republic

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First published: 12 September 2007
Citations: 52

Dedicated to Professor Nina Berova on the occasion of her significant anniversary and her receiving the Chirality Medal 2007.

Abstract

The development of density functional theory (DFT) methods for the calculation of vibrational circular dichroism (VCD), electronic circular dichroism (ECD), and transparent spectral region optical rotation (OR) has revolutionized the determination of the absolute configurations (ACs) of chiral molecules using these chiroptical properties. We report the concerted application of DFT calculations of VCD, ECD, and OR to the determination of the ACs of the isoschizozygane alkaloid natural products, isoschizogaline, and isochizogamine, whose ACs have not previously been determined. The ACs of naturally occurring (−)‐isoschizogaline and (−)‐isoschizogamine, are both determined definitively to be 2R, 7R, 20S, 21S. Chirality, 2008. © 2007 Wiley‐Liss, Inc.

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