Kotha, Sambasivarao ; Ghosh, Arun Kumar (2004) A Diels-Alder approach for the synthesis of highly functionalized benzo-annulated indane-based α-amino acid derivatives via a sultine intermediate Tetrahedron Letters, 45 (14). pp. 2931-2934. ISSN 0040-4039
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tetlet.2004.02.060
Abstract
The synthesis of various highly functionalized benzo-annulated indane-based α-amino acid (AAA) derivatives are reported via a [4+2] cycloaddition strategy using a sultine derivative, containing an AAA moiety, as a reactive diene component. By adopting this strategy, a new α,α-dialkylated indane-based C60 fullerene containing a constrained AAA unit is reported.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Diels-Alder Cycloaddition; Sultine; DDQ Oxidation; Amino Acid; Fullerene |
| ID Code: | 65158 |
| Deposited On: | 15 Oct 2011 11:41 |
| Last Modified: | 15 Oct 2011 11:41 |
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