Facile Entry to the Zaragozic Acids. Asymmetric Total Synthesis of 6,7-Dideoxysqualestatin H5
- 1 October 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (22) , 7592-7593
- https://doi.org/10.1021/jo981684k
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Biological Activities of Novel Zaragozic Acids, the Potent Inhibitors of Squalene Synthase, Produced by the Fungus, Mollisia sp. SANK 10294.The Journal of Antibiotics, 1997
- DISCOVERY, BIOSYNTHESIS, AND MECHANISM OF ACTION OF THE ZARAGOZIC ACIDS: Potent Inhibitors of Squalene SynthaseAnnual Review of Microbiology, 1995
- Synthesis of Zaragozic Acid A/Squalestatin S1Chemistry – A European Journal, 1995
- Carbohydrate-Based Strategy for the Synthesis of Zaragozic Acid via a Novel Lewis Acid-Mediated Reaction of an .alpha.-Acetoxy SulfideThe Journal of Organic Chemistry, 1995
- Total Synthesis of Zaragozic Acid A/Squalestatin S1Angewandte Chemie International Edition in English, 1994
- The squalestatins, novel inhibitors of squalene synthase produced by a species of Phoma. V. Minor metabolites.The Journal of Antibiotics, 1994
- Zaragozic acids: a family of fungal metabolites that are picomolar competitive inhibitors of squalene synthase.Proceedings of the National Academy of Sciences, 1993
- Competitive inhibition of squalene synthetase by squalestatin 1.The Journal of Antibiotics, 1993
- The isolation and structure elucidation of zaragozic acid C, a novel potent squalene synthase inhibitor.Tetrahedron, 1992
- The squalestatins, novel inhibitors of squalene synthase produced by a species of Phoma. II. Structure elucidation.The Journal of Antibiotics, 1992