Absolute stereochemistry and synthesis of aplyronines B and C, the congeners of aplyronine A, a potent antitumor substance of marine origin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Aplyronine A, a potent antitumor substance and the congeners aplyronines B and C isolated from the sea hare Aplysia kurodai
2. Further studies on aplyronine A, an antitumor substance isolated from the sea hare Aplysia kurodai
3. Studies on the stereochemistry of aplyronine A: Determination of the stereochemistry of the C21C34 fragment
4. Absolute Stereochemistry of Aplyronine A, a Potent Antitumor Substance of Marine Origin
5. Synthetic Studies on Aplyronine A, a Potent Antitumor Substance of Marine Origin: Stereocontrolled Synthesis of the C21–C34 Segment
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1. Synthesis and Biological Activities of Aplyronine A Analogues toward the Development of Antitumor Protein–Protein Interaction Inducers between Actin and Tubulin: Conjugation of the C1–C9 Macrolactone Part and the C24–C34 Side Chain;ACS Omega;2019-05-16
2. Citric acid mediated catalytic osmylation/oxidative cleavage of electron deficient olefins: a vinyl sulfone study;Tetrahedron Letters;2015-07
3. Recent Progress in The Synthetic Study of an Antitumor Marine Macrolide Aplyronine A and Related Molecules;HETEROCYCLES;2015
4. Antitumor Effects of Sea Hare-Derived Compounds in Cancer;Handbook of Anticancer Drugs from Marine Origin;2014-11-28
5. Mollusks-2;Encyclopedia of Marine Natural Products;2014-08-07
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