Jayakanthan, K. ; Vankar, Yashwant D. (2005) Synthesis of conformationally constrained C-glycosyl α- and β-amino acids and sugar-carbamino sugar hybrids via Diels-Alder reaction Organic Letters, 7 (24). pp. 5441-5444. ISSN 1523-7060
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Official URL: http://pubs.acs.org/doi/abs/10.1021/ol052190u
Related URL: http://dx.doi.org/10.1021/ol052190u
Abstract
Sugar-derived dienes undergo Diels-Alder reactions with methyl α-nitro acrylate and ethyl β-nitro acrylate to form the corresponding cycloadducts which have been converted into conformationally constrained C-glycosyl α- and β-amino acids. Further, these β-amino acids are converted into sugar-carbamino sugar hybrid molecules.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to American Chemical Society. |
| ID Code: | 58162 |
| Deposited On: | 31 Aug 2011 06:38 |
| Last Modified: | 31 Aug 2011 06:38 |
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