2-Acetoxyacrylonitrile: use as electrophile equivalent to acetaldehyde in the asymmetric Michael reaction using chiral imines
✍ Scribed by Laurent Keller; Cheikhou Camara; Antonio Pinheiro; Françoise Dumas; Jean d'Angelo
- Book ID
- 104211515
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 81 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The asymmetric Michael addition reaction between a variety of chiral imines and 2-acetoxyacrylonitrile, an electrophile equivalent to acetaldehyde, was reported. The resulting adducts were obtained in fair yields and with de and ee ]95%.
📜 SIMILAR VOLUMES
A novel asymmetric synthesis of 1-aryl-1,2,3,4-tetrahy-sodium in liquid ammonia and ammonium cerium(IV) nitrate, respectively, to yield the primary amines 35 and 36. The acid-droisoquinolines has been developed. The key step in this synthesis is the diastereoselective addition of homochiral (2-catal