Stereochemistry of Sagittamide A from Residual Dipolar Coupling Enhanced NMR-Reference-Cited by-同舟云学术

Stereochemistry of Sagittamide A from Residual Dipolar Coupling Enhanced NMR

Published:2007-11-14 Issue:49 Volume:129 Page:15114-15115
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Schuetz Anne¹,Junker Jochen¹,Leonov Andrei¹,Lange Oliver F.¹,Molinski Tadeusz F.¹,Griesinger Christian¹

Affiliation:

1. Department of NMR Based Structural Biology, Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Göttingen, Germany, Department of Biochemistry, University of Washington, J Wing, Health Sciences Building, Box 357350, Seattle, Washington 98195, and Department of Chemistry and Biochemistry and Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja075876l

Reference17 articles.

1. Sagittamides A and B. Polyacetoxy Long-Chain Acyl Amino Acids from a Didemnid Ascidian

2. Assignment of the absolute configuration of blasticidin A and revision of that of aflastatin A

3. Progressive−Convergent Elucidation of Stereochemistry in Complex Polyols. The Absolute Configuration of (−)-Sagittamide A

4. Stereochemical Determination of Acyclic Structures Based on Carbon−Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products

5. Universal NMR Databases for Contiguous Polyols

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