𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Synthesis of New Enantiopure γ-Amino Alcohols: Their Use as Catalysts in the Alkylation of Benzaldehyde by Diethylzinc.

✍ Scribed by S. CICCHI; S. CREA; A. GOTI; A. BRANDI


Publisher
John Wiley and Sons
Year
2010
Weight
33 KB
Volume
28
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis


Synthesis of New Enantiopure γ-Amino Alcohols: Their Use as Catalysts in the Alkylation of Benzaldehyde by Diethylzinc.

-Seven γ-amino alcohols are prepared by a convenient method based on 1,3-dipolar cycloaddition of the nitrone (I) to olefins. Among them the alcohols (VI) and (VIIa) are best catalysts in zinc mediated alkylation of benzaldehyde. However, only modest enantioselectivity is observed.


📜 SIMILAR VOLUMES


Synthesis of new pryridyl alcohols and t
✍ Qianyong Xu; Xiaoming Wu; Xinfu Pan; Albert S. C. Chan; Teng-Kuei Yang 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 62 KB 👁 1 views

## Abstract Optically active new pyridyl alcohols **1–4**, which can be easily synthesized by the reaction of (+)‐camphor or (−)‐menthone with lithiated pyridine derivatives, were applied as chiral ligands in the asymmetric addition of diethylzinc to aldehydes. Good yields with up to 94.0%enantiome