Podocarpane-to-spongian skeleton conversion. Synthesis of (+)-isoagatholactone and (–)-spongia-13(16),14-diene
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1996/P1/P19960002193
Reference23 articles.
1. Stereoselective synthesis of the enantiomer of the novel marine diterpene isoagatholactone, ent-13(16),14-spongiadien-12.alpha.-ol, and the parent hydrocarbon isocopalane from methyl isocopalate
2. Total syntheses of (±)-isoagatholactone and (±)-12α-hydroxyspongia-13(16),14-dien
3. Stereoselective total syntheses of (±)-isoagatholactone and (±)-12α-hydroxyspongia-13(16),14-diene, two marine sponge metabolites
4. Spongian furanoditerpenes: An intramolecular radical approach
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