X-ray Crystallography and Unexpected Chiroptical Properties Reassign the Configuration of Haliclonadiamine-Reference-Cited by-同舟云学术

X-ray Crystallography and Unexpected Chiroptical Properties Reassign the Configuration of Haliclonadiamine

Published:2020-01-27 Issue:6 Volume:142 Page:2755-2759
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liu Hong-Bing¹,Imler Gregory H.²,Baldridge Kim K.³^ORCID,O’Connor Robert D.¹,Siegel Jay S.³^ORCID,Deschamps Jeffrey R.²,Bewley Carole A.¹^ORCID

Affiliation:

1. Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0820, United States

2. Center for Biomolecular Science and Engineering, Naval Research Laboratory, Code 6930, Washington, D.C. 20375, United States

3. Health Science Platform, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P.R. China

Funder

Ministry of Science and Technology of the People's Republic of China

National Institute of Diabetes and Digestive and Kidney Diseases

Qian Ren Scholar Program of China

Synergistic Innovation Center of Chemical Science and Engineering

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.9b12926

Reference26 articles.

1. Papuamine, an antifungal pentacyclic alkaloid from a marine sponge, Haliclona sp

2. Haliclonadiamine, an antimicrobial alkaloid from the sponge Haliclona SP

3. Total Synthesis of (+)-Papuamine: An Antifungal Pentacyclic Alkaloid from a Marine Sponge, Haliclona sp.

4. Total synthesis of (+)-papuamine: determination of the absolute stereochemistry of the natural product

5. Total Synthesis of Papuamine via a Stereospecific Intramolecular Imino Ene Reaction of an Allenylsilane

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