Biscembranoids Formed from an α,β-Unsaturated γ-Lactone Ring as a Dienophile: Structure Revision and Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra-Reference-Cited by-同舟云学术

Biscembranoids Formed from an α,β-Unsaturated γ-Lactone Ring as a Dienophile: Structure Revision and Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra

Published:2013-02-28 Issue:7 Volume:78 Page:3113-3119
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Jia Rui¹²,Kurtán Tibor³,Mándi Attila³,Yan Xiao-Hong¹,Zhang Wen⁴,Guo Yue-Wei¹

Affiliation:

1. State Key Laboratory of Drug Research, Institute of Materia Medica, Chinese Academy of Sciences, Zu Chong Zi Rd. 555, Zhangjiang Hi-Tech Park, Shanghai 201203, P. R. China

2. College of Fisheries and Life Science, Water Environment & Ecology Engineer Research Center, Shanghai Ocean University, Shanghai 201306, P. R. China

3. Department of Organic Chemistry, University of Debrecen, P.O. Box 20, H-4010 Debrecen, Hungary

4. Research Center for Marine Drugs, School of Pharmacy, Second Military Medical University, 325 Guo-He Road, Shanghai 200433, P. R. China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo400069n

Reference38 articles.

1. The structure of methyl isosartortuoate, a novel tetracyclic tetraterpenoid from the soft coral Sarcophyton tortuosum

2. A novel chlorinated biscembranoid from the marine soft coral Sarcophyton glaucum

3. Difference CD spectrum : the absolute configuration of methyl sarcophytoate

4. Studies of Australian Soft Corals, XLIX. A New Biscembranoid and Its Probable Biosynthetic Precursors from the Soft Coral Sarcophyton tortuosum

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