Stereoselective Cyclopropanation and Ring-Opening: Application to the Synthesis of Pure (S)-2-Methyl-3-arylpropylamines. -A short synthesis (6 steps) of the (S)-enantiomers (I) and (II) of the fungicides fenpropimorph and fenpropidine is presented. The required trans-isomers (VI) of the cyclopropan
✦ LIBER ✦
ChemInform Abstract: Ring-Opening Hydrofluorination of 2,3- and 3,4-Epoxy Amines by HBF4·OEt2: Application to the Asymmetric Synthesis of (S,S)-3-Deoxy-3-fluorosafingol.
✍ Scribed by Alexander J. Cresswell; Stephen G. Davies; James A. Lee; Melloney J. Morris; Paul M. Roberts; James E. Thomson
- Publisher
- John Wiley and Sons
- Year
- 2011
- Weight
- 33 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
The reaction allows a simple, efficient, and highly stereoselective (< 98% d.e.) access to synthetically and biologically important fluorohydrins.
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