The total synthesis of the new sesquiterpenoid (±)-fulvanin 1 / Sollasin a
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Sesquiterpene-Derived Metabolites from the Deep Water Marine Sponge Poecillastra sollasi
2. Paniceins and Related Sesquiterpenoids from the Mediterranean Sponge Reniera fulva
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4. A one-flask multicomponent annulation reaction as the key step in a total synthesis of spirobicyclic (±)-β-vetivone
5. Transannular Interactions. III. Synthesis and Assignment of Configurations in the cis- and trans-5-Cyclodecen-1-yl System1
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Porifera (Sponges)-5;Encyclopedia of Marine Natural Products;2014-08-07
2. ChemInform Abstract: The Total Synthesis of the New Sesquiterpenoid (.+-.)-Fulvanin 1/ Sollasin a.;ChemInform;2010-08-17
3. Total Synthesis of Sollasin a and Sollasin d via Photocycloaddition of Methyl 2,4-Dioxopentanoate to Methyl E-2-Methyl-2-butenoate;Chemistry Letters;1998-02
4. An approach to the C(17)–C(24) fragment of bryostatins: applications of stereoselective trisubstituted alkene formation by palladium(0) catalysed coupling of enol acetates and vinylic bromides;Journal of the Chemical Society, Perkin Transactions 1;1998
5. An approach to the C(10)–C(16) fragment of the bryostatins: stereoselective exocyclic double-bond formation by vinyl radical cyclization;Journal of the Chemical Society, Perkin Transactions 1;1998
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