Diels–Alder Reactions of 5,6-Dihydro-2(1H)-pyridones
✍ Scribed by Núria Casamitjana; Virginia López; Angela Jorge; Joan Bosch; Elies Molins; Anna Roig
- Book ID
- 108370830
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 278 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
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Diels-Alder Reactions of 5,6-Dihydro-2(1H)-pyridones. Preparation of Partially Reduced cis-Isoquinolones and cis-3,4-Disubstituted Piperidines. -Dihydropyridones (I) and (IV) undergo thermal or Lewis acid induced Diels-Alder reaction with various butadienes to give cisisoquinolone derivatives. cis-
A tandem Diels-Alder cyclization/aromatization of 5-vinyl-2,3-dihydro-4-pyridones and various dienophiles is reported. The intermediate Diels-Alder cycloadduct undergoes an elimination/aromatization to provide b-amino-ketones, b-amino-alcohols, and unnatural amino acids containing useful functionali
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