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Efficient Resolution of (.+-.)-1-(9-Anthryl)ethylamine.

✍ Scribed by Marin Roje; Zdenko Hamersak; Vitomir Sunjic

Book ID
101935939
Publisher
John Wiley and Sons
Year
2003
Weight
60 KB
Volume
34
Category
Article
ISSN
0931-7597

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✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

πŸ“œ SIMILAR VOLUMES

Chemoenzymatic synthesis and properties
Chemoenzymatic synthesis and properties of Schiff bases containing (R)-1-(9-anthryl)ethylamine
✍ Marin Roje; Vitomir Ε unjiΔ‡ πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 113 KB

## Abstract Racemic 1‐(9‐anthryl)ethylamine (**10**), obtained in 70% overall yield from commercial 9‐cyanoanthracene, was kinetically resolved by the __Candida antarctica A__ lipase‐catalyzed acetylation with isopropyl acetate as acyl donor, affording (__R__)‐(+)‐**10** with 95.8% enantiomeric exc

Preparation of 1-(9-anthryl)-ethanol and
Preparation of 1-(9-anthryl)-ethanol and 9-anthryloxirane via catalytic enantioselective reduction of prochiral 9-anthryl ketones
✍ I. Reiners; J. Martens πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 English βš– 120 KB

Enantioselective reduction of prochiral 9-anthryl ketones to the corresponding chiral alcohols proceeds with high enantiomeric excess. The chiral alcohol 1-(9-anthryl)-2-bromo-ethanol can be converted to the corresponding chiral oxirane. (~