## Abstract The tandem‐Knoevenagel‐hetero‐Diels‐Alder reaction of the chiral enantiomerically pure monoterpene glucoside secologanin (1) with 1,3‐dicarbonyl compounds 6a–d and the analogous compounds 11a–b in the presence of ethylenediammonium diacetate as catalyst leads to the bridged cycloadducts
Asymmetric synthesis of the C-26-C-32 tetrahydropyran — moiety of Swinholide A by hetero-Diels-Alder reaction
✍ Scribed by Johann Mulzer; Frank Meyer; Jürgen Buschmann; Peter Luger
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 189 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
The tetrahydropyranone 3, representing a pentacyclic C 4 -C 32 segment of the phorboxazoles, was obtained by a complex hetero Diels-Alder (HDA) coupling performed between the 2-siloxydiene 23 and the oxazole aldehyde 4, mediated by the chiral tridentate Cr(III) catalyst 14. In preliminary studies, t
Diastereomerically pure oxazolo[3, pyrimidines can be readily prepared by the reaction of alkenyloxazolines with isocyanates. These compounds undergo epimerisation upon prolonged heating. The mechanism of this transformation has been investigated experimentally and computationally.