Total Synthesis of the Squalene Synthase Inhibitor Zaragozic Acid C by a Carbonyl Ylide Cycloaddition Strategy
- 4 November 2003
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 42 (43), 5351-5355
- https://doi.org/10.1002/anie.200352629
Abstract
No abstract availableThis publication has 49 references indexed in Scilit:
- Carbonyl YlidesPublished by Wiley ,2002
- Facile Entry to the Zaragozic Acids. Asymmetric Total Synthesis of 6,7-Dideoxysqualestatin H5The Journal of Organic Chemistry, 1998
- Facile and Efficient Preparation of a C-1 Side Chain Equivalent of Zaragozic Acid C.CHEMICAL & PHARMACEUTICAL BULLETIN, 1998
- Total Synthesis of the Squalene Synthase Inhibitor Zaragozic Acid CSynlett, 1997
- Saragossasäure‐TotalsynthesenAngewandte Chemie, 1995
- Asymmetric Synthesis of the Squalene Synthase Inhibitor Zaragozic Acid CJournal of the American Chemical Society, 1994
- Total Synthesis of Zaragozic Acid A/Squalestatin S1Angewandte Chemie International Edition in English, 1994
- Totalsynthese von Saragossasäure A/Squalestatin S1Angewandte Chemie, 1994
- Tandem cyclization-cycloaddition reaction of rhodium carbenoids. Scope and mechanistic details of the processJournal of the American Chemical Society, 1990
- Reaction of Diazo Ketones in the Presence of Metal Chelates. VII. 1,3-Dipolar Cycloaddition of 1-Methoxybenzo[c]pyrylium-4-olate with Acetylenic DipolarophilesBulletin of the Chemical Society of Japan, 1979