ChemInform Abstract: Ready Access to Enantiopure 5-Substituted-3-pyrrolin-2-ones from N-Benzyl-2,3-O-isopropylidene-D-glyceraldehyde Nitrone (BIGN).
โ Scribed by P. MERINO; E. CASTILLO; S. FRANCO; F. L. MERCHAN; T. TEJERO
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Ready Access to Enantiopure 5-Substituted-3-pyrrolin-2-ones from N-Benzyl-2,3-O-isopropylidene-D-glyceraldehyde Nitrone (BIGN).
-A short and efficient route to the title compounds is developed. These pyrrolinones are useful synthetic synthons and can be employed for the preparation of highly functionalized pyrrolidines.
๐ SIMILAR VOLUMES
Nucleophilic Additions of Grignard Reagents to N-Benzyl-2,3-O-isopropylidene-D-glyceraldehyde Nitrone (BIGN). Synthesis of (2S,3R) and (2S,3S)-3-Phenylisoserine. -The addition of Grignard reagents to the nitrone (I) proceeds with high anti or syn selectivity depending on the Lewis acid used. The re