Studies Directed toward the Total Synthesis of Azaspiracid: Stereoselective Construction of C1−C12, C13−C19, and C21−C25 Fragments
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of Mississippi, University, Mississippi 38677
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol006674w
Reference25 articles.
1. Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, Mytilus edulis
2. Two analogs of azaspiracid isolated from mussels, Mytilus edulis, involved in human intoxication in Ireland
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