(+)-Camphor-derived tri- and tetradentate amino alcohols; synthesis and application as ligands in the nickel catalyzed enantioselective conjugate addition of diethylzinc
✍ Scribed by AndréH.M. de Vries; Rosalinde Imbos; Ben L. Feringa
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 455 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
✦ Synopsis
Several novel tri-and tetradentate amino alcohol ligands, all derived from (+)-camphor, have been synthesized by using specific N-alkylation procedures. The amino alcohols were employed as chiral ligands in the nickel catalyzed conjugate additions of diethylzinc to chalcone and cyclohexenone as model substrates. For the acyclic enone enantioselectivities up to 83% were achieved. (~) 1997 Elsevier Science Ltd
📜 SIMILAR VOLUMES
## Abstract A new class of chiral β‐amino disulfides was synthesized from readily available and inexpensive starting materials by a straightforward method and their abilities as ligands were examined in the enantioselective addition of diethylzinc to aldehydes. Enantiomeric excesses of up to 99% ha
Two generally applicable routes for the synthesis of chiral amino alcohols embodying the bispidine framework have been developed. In linear route A the bispidine framework is built up successively from chiral primary amines via intermediate formation of a piperidinone and a bispidinone. In convergen