the optical rotation ([a] D 25 ) of compound 6 should read +19.9 (c 1.0, CHCl 3 ) instead of À 19.9 (c 1.3, CHCl 3 ). Hence the absolute configurations of 2, 36, 6, 7 and 8 should correspond to those of the enantiomers. The authors apologize for this error. The corresponding corrections have been ma
A Catalytic and Enantioselective Synthesis of trans-2-Amino-1- aryltetralins
✍ Scribed by Saumen Hajra; Biswajit Maji; Dipakranjan Mal
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 215 KB
- Volume
- 351
- Category
- Article
- ISSN
- 1615-4150
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✦ Synopsis
Abstract
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The bis‐oxazoline‐copper complex‐catalyzed aziridination of alkenes followed by an intramolecular Friedel–Crafts alkylation of the tethered and in situ generated aziridine provides a one‐pot, general and efficient method for the synthesis of trans‐2‐amino__‐__1‐aryltetralins from a mixture of 2‐ arylethylstyrenes (E/Z≤85:15) with excellent dia‐ stereo‐ (dr>99:1) and enantioselectivities (up to 92% ee).
📜 SIMILAR VOLUMES
Scheme 1. Retrosynthesis of (+)-trans-dihydronarciclasine 1 (PG = protecting group).
The enantioselective synthesis of a-aminoand a-hydroxy phosphonates by catalytic processes has attracted considerable interest in the last few years, not least because of the pharmaceutical interest in such compounds. This article contains a compilation of the asymmetric synthesis methods developed