Access to the core structure of aurisides by a ring-closing metathesis/transannular ketalisation sequence
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference62 articles.
1. Aurisides A and B, Cytotoxic Macrolide Glycosides from the Japanese Sea Hare Dolabella auricularia
2. Kornprobst, J.-M. In Substances naturelles d’origine marine, Tec&Doc ed., Paris, 2005, pp 1313–1315.
3. Antineoplastic Agents. 510. Isolation and Structure of Dolastatin 19 from the Gulf of California Sea Hare Dolabella auricularia
4. Total Synthesis and Stereochemical Reassignment of (+)-Dolastatin 19
5. Synthesis of the Aglycon of Aurisides A and B, Cytotoxic Macrolide Glycosides of Marine Origin
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1. Stereoselective Synthesis of γ-Butyrolactones Subunit of Polycavernoside A;Journal of Heterocyclic Chemistry;2018-07-03
2. Olefin Ring‐Closing Metathesis;Organic Reactions;2016-02
3. Mollusks-2;Encyclopedia of Marine Natural Products;2014-08-07
4. The chemistry of the carbon–transition metal double and triple bond: Annual survey covering the year 2009;Coordination Chemistry Reviews;2011-01
5. Stereocontrolled Synthesis of the Highly Functionalized Core Structure of Aurisides by Ring-Closing Metathesis;European Journal of Organic Chemistry;2010-06-02
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