Diastereoselective Diels-Alder reactions of nonracemic 3- and 4-amino furans bound to polystyrene. A comparison of these reactions to their solution state analogues
Open Access
- 25 March 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (13) , 2133-2136
- https://doi.org/10.1016/0040-4039(96)00208-0
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Diastereoselective Diels-Alder Reactions of a Furan Substituted with a Proline Derived AuxiliarySynlett, 1995
- Enantioselective Synthesis of (+)-CyclophellitolThe Journal of Organic Chemistry, 1995
- Short Enantioselective Synthesis of (-)-Ovalicin, a Potent Inhibitor of Angiogenesis, Using Substrate-Enhanced Catalytic Asymmetric DihydroxylationJournal of the American Chemical Society, 1994
- 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
- Diastereoselective Diels-Alder Reactions Using Furan Substituted with a Nonracemic AmineThe Journal of Organic Chemistry, 1994
- Total synthesis of (–)-ovalicine fromL-quebrachitolJournal of the Chemical Society, Chemical Communications, 1994
- Esperamicins, a novel class of potent antitumor antibiotics. 3. Structures of esperamicins A1, A2, and A1bJournal of the American Chemical Society, 1987
- Esperamicins, a novel class of potent antitumor antibiotics. I. Physico-chemical data and partial structure.The Journal of Antibiotics, 1985
- Total synthesis of (+-)-fumagillinJournal of the American Chemical Society, 1972