Enantiomeric Discorhabdin Alkaloids and Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra-Reference-Cited by-同舟云学术

Enantiomeric Discorhabdin Alkaloids and Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra

Published:2008-10-15 Issue:22 Volume:73 Page:9133-9136
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Grkovic Tanja¹,Ding Yuanqing¹,Li Xing-Cong¹,Webb Victoria L.¹,Ferreira Daneel¹,Copp Brent R.¹

Affiliation:

1. Department of Chemistry, The University of Auckland, Private Bag 92019, Auckland, New Zealand, Department of Pharmacognosy and National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, and National Institute of Water & Atmospheric Research (NIWA) Ltd, Private Bag 14-901, Kilbirnie, Wellington, New Zealand

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo801622n

Reference27 articles.

1. Pyrroloiminoquinone and related metabolites from marine sponges

2. Discorhabdin W, the First Dimeric Discorhabdin

3. Taxonomic revision of the genusLatrunculiaDu Bocage (Porifera: Demospongiae: Latrunculiidae) in New Zealand

4. Revision of the genus Latrunculia du Bocage, 1869 (Porifera: Demospongiae: Latrunculiidae) with descriptions of new species from New Caledonia and the Northeastern Pacific

5. Discorhabdin C, a highly cytotoxic pigment from a sponge of the genus Latrunculia

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