Synthesis, resolution and anticonvulsant activity of chiral N-1′-ethyl,N-3′-(1-phenylethyl)-(R,S)-2′H,3H,5′H-spiro-(2-benzofuran-1,4′-imidazolidine)-2′,3,5′-trione diastereomers
✍ Scribed by Ishwar R. Sadarangani; Souful Bhatia; Daniel Amarante; Istvan Lengyel; Ralph A. Stephani
- Book ID
- 113496687
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 268 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0960-894X
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📜 SIMILAR VOLUMES
Cycloaddition of a (−)-menthone-derived nitrone to racemic but-3-en-2-ol led to two spirobicyclic heterocycles, with opposite configurations at the C atom attached to the OH group. This paper describes the __S__ epimer of the 1-hydroxyethyl substituent in imidazoisoxazole C~17~H~30~N~2~O~3~, (I). Th
Cycloaddition of a (−)-menthone-derived nitrone to racemic but-3-en-2-ol led to two spirobicyclic heterocycles, with opposite configurations at the C atom attached to the OH group. This paper describes the __R__ epimer of the 1-hydroxyethyl substituent in imidazoisoxazole C~17~H~30~N~2~O~3~, (I). Th