Cytotoxicity and actin depolymerizing activity of aplyronine A, a potent antitumor macrolide of marine origin, and the natural and artificial analogs
- 4 February 1997
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 7 (3) , 269-274
- https://doi.org/10.1016/s0960-894x(96)00620-8
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Aplyronine A, a Potent Antitumor Substance of Marine Origin, Aplyronines B and C, and Artificial Analogues: Total Synthesis and Structure−Cytotoxicity RelationshipsThe Journal of Organic Chemistry, 1996
- Absolute stereochemistry and synthesis of aplyronines B and C, the congeners of aplyronine A, a potent antitumor substance of marine originTetrahedron Letters, 1995
- Total Synthesis of Aplyronine A, a Potent Antitumor Substance of Marine OriginJournal of the American Chemical Society, 1994
- Absolute Stereochemistry of Aplyronine A, a Potent Antitumor Substance of Marine OriginJournal of the American Chemical Society, 1994
- Further studies on aplyronine A, an antitumor substance isolated from the sea hare Aplysia kurodaiTetrahedron Letters, 1993
- Aplyronine A, a potent antitumor substance and the congeners aplyronines B and C isolated from the sea hare Aplysia kurodaiJournal of the American Chemical Society, 1993
- Studies on the stereochemistry of aplyronine A: Determination of the stereochemistry of the C21C34 fragmentTetrahedron Letters, 1993
- Studies in polypropionate synthesis: high π-face selectivity in syn aldol reactions of tin(II) enolates from (R)- and (S)-1-benzyloxy-2-methylpentan-3-one.Tetrahedron Letters, 1992
- A Rapid Esterification by Means of Mixed Anhydride and Its Application to Large-ring LactonizationBulletin of the Chemical Society of Japan, 1979
- Reduction of Organic Compounds with NaBH4-Transition Metal Salt Systems. IV. Selective Hydrogenation of Olefines in Unsaturated EstersCHEMICAL & PHARMACEUTICAL BULLETIN, 1971