A completely stereoselective intramolecular diels-alder reaction in the substituted cyclohexanol series
β Scribed by A. Alexakis; D. Jachiet; L. Toupet
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 475 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
Zn the preceding article' we have efficiently
π SIMILAR VOLUMES
Azabutadienes f Isoxazoles f Tetrahydropyridines 1 Diels-Alder reactions / Sequential transformations Condensation of aldehydes 1 ae with 5-amino-3-methylisoxazole (4) gives the corresponding imines 5a-e with a 2-aza-1,3-butadiene moiety, which cyclize selctively, e.g. 5a to form the trans-fused tet
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