Toward Computing Relative Configurations: 16-epi-Latrunculin B, a New Stereoisomer of the Actin Polymerization Inhibitor Latrunculin B-Reference-Cited by-同舟云学术

Toward Computing Relative Configurations: 16-epi-Latrunculin B, a New Stereoisomer of the Actin Polymerization Inhibitor Latrunculin B

Published:2002-06-01 Issue:25 Volume:124 Page:7405-7410
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hoye Thomas R.¹,Ayyad Seif-Eldin N.¹,Eklov Brian M.¹,Hashish Nadia E.¹,Shier W. Thomas¹,El Sayed Khalid A.¹,Hamann Mark T.¹

Affiliation:

1. Contribution from the Departments of Chemistry and Medicinal Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, Department of Pharmacognosy, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, and Chemistry Department, Faculty of Science, Mansoura University, New Dammiatta, Egypt

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja025734l

Reference24 articles.

1. Structures and absolute configurations of the marine toxins, latrunculin A and laulimalide

2. (b) Hoye, T. R.; Zhao, H.J. Org. Chem.Published on web 05/14/2002.

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