Kotha, Sambasivarao ; Ghosh, Arun Kumar (2004) Cycloaddition approach to benzo-annulated indane-based α-amino acid derivatives Tetrahedron, 60 (48). pp. 10833-10841. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2004.09.051
Abstract
Synthesis of various benzo-annulated indane-based α-amino acid (AAA) derivatives are reported via a [4+2] and [2+2+2] cycloaddition reactions as key steps. Here, o-xylylene based AAA moiety has been used as a reactive intermediate and by adopting this strategy various indane-based constrained AAA derivatives are prepared.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Amino Acids and Derivatives; Fullerenes; Sulfur Heterocycles; Cycloadditions; Diels-Alder Reactions |
| ID Code: | 65148 |
| Deposited On: | 15 Oct 2011 11:41 |
| Last Modified: | 15 Oct 2011 11:41 |
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