A stereocontrolled synthesis of (2R,3R,5R,13S,14R)- (+)-Aplidiasphingosine, a marine terpenoid
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (33) , 3391-3394
- https://doi.org/10.1016/s0040-4039(00)87623-6
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Synthesis of both 2,3-Tetrahedron Letters, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Synthesis of the polyether antibiotic monensin. 2. Preparation of intermediatesJournal of the American Chemical Society, 1980
- Stereoselective Synthesis of Z‐α,β‐Unsaturated AldehydesAngewandte Chemie International Edition in English, 1979
- An alternative synthesis of (2R,6R)-(-)-2,6,10-trimethylundecyl bromide, the key intermediate in the synthesis of natural .ALPHA.-tocopherol.Agricultural and Biological Chemistry, 1979
- Aplidiasphingosine, an antimicrobial and antitumor terpenoid from an Aplidium species (marine tunicate)Journal of the American Chemical Society, 1978
- Stereoselective epoxidation of acyclic olefinic carboxylic acids via iodolactonizationJournal of the American Chemical Society, 1978
- Synthesis of the Valeriana waalichi hydrocarbon sesquifenchene. Route to specifically functionalized 7,7-disubstituted bicyclo[2.2.1]heptane derivativesThe Journal of Organic Chemistry, 1975
- A New, Highly Stereoselective Synthesis of alltrans-GeranylgeraniolSynthesis, 1974
- Improved procedure for oxidations with the chromium trioxide-pyridine complexThe Journal of Organic Chemistry, 1970