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Lewis acid-catalyzed hetero Diels–Alder cycloadditions of 3-alkyl, 3-phenyl and 3-carboxylated 2H-azirines
✍ Scribed by Colin A Ray; Erik Risberg; Peter Somfai
- Book ID
- 104232086
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 65 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Activation by Lewis acids of 3-alkyl and 3-phenyl 2H-azirines promotes their participation in hetero Diels-Alder reactions with a variety of dienes. This methodology circumvents the previous requirement of an electron-withdrawing carboxyl moiety at the 3-position of the 2H-azirine.
📜 SIMILAR VOLUMES
Me2AICI -and TiCl4-catalyzed asymmetric hetero Diels-Alder cycloaddition reactions of 2,4-diphenyl-l-thiabuta-l,3-diene with (S)-N-acryloyl-and (S)-N-crotonoyl-4-benzyl-l,3-oxazolidin-2one dienophiles are described in which not only the sense of the n-facial selectivity but also the degree dramatica