
Please use this identifier to cite or link to this item:
http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/2883| Title: | Organocatalytic enantioselective synthesis of C3 functionalized indole derivatives |
| Authors: | Kaur, J. Islam, N. Kumar, A. Bhardwaj, V. K. Chimni, S. S. |
| Keywords: | Organocatalysis Michael addition reaction Indolylnitroalkenes Enantioselective DFT |
| Issue Date: | 4-Oct-2021 |
| Abstract: | A highly enantioselective Michael addition reaction of indolylnitroalkenes with 1,3-dicarbonyl compounds has been developed to obtain enantiomerically enriched 3-(2-nitro-1-(1-tosyl-1H-indol-3-yl) ethyl)pentane-2,4-dione derivatives in up to 98% ee using BnCPN as an organocatalyst. The transition state structure has been predicted using DFT calculation |
| URI: | http://localhost:8080/xmlui/handle/123456789/2883 |
| Appears in Collections: | Year-2016 |
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| Full Text.pdf | 1.15 MB | Adobe PDF | View/Open Request a copy |
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