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ChemInform Abstract: Ready Access to Enantiopure 5-Substituted-3-pyrrolin-2-ones from N-Benzyl-2,3-O-isopropylidene-D-glyceraldehyde Nitrone (BIGN).

โœ 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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โœฆ 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.


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: Nucleophilic Additi
โœ P. MERINO; E. CASTILLO; S. FRANCO; F. L. MERCHAN; T. TEJERO ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 38 KB ๐Ÿ‘ 2 views

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