X ray study of sesquiterpene constituents of the alga L obtusa leads to structure revision
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference3 articles.
1. Evidence for the biogenesis of halogenated chamigrenes from the red alga laurencia obtusa
2. Revised structure of caespitol and its correlation with isocaespitol
3. Nidifocene: a reassignment of structure
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