Diastereoselective synthesis and 1H and 13C NMR study of 4-acetyl-2,6-diaroyl-3,5-diaryl-4-ethoxycarbonylthiane-1,1-dioxides
✍ Scribed by S. Renuga; S. Selvaraj; S. Perumal; A. Lycka; M. Gnanadeebam
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 98 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.897
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✦ Synopsis
Abstract
Conjugate addition of ethyl acetoacetate to 2,2′‐sulfonylbis(1,3‐diarylprop‐2‐en‐1‐ones) afforded a diastereom‐eric mixture (in a ratio of ∼65:35) of 4‐acetyl‐2,6‐diaroyl‐3,5‐diaryl‐4‐ethoxycarbonylthiane‐1,1‐dioxides differing in configuration at C‐4. The stereochemistry of the diastereomeric thianes was established by ^1^H, ^13^C and 2D NMR spectroscopic techniques such as H,H‐COSY, C,H‐COSY and NOESY. Copyright © 2001 John Wiley & Sons, Ltd.
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