Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/4476| Title: | Azobenzene-based unnatural amino acid scaffolds via a Pd(II)-catalyzed C(sp3)–H arylation strategy |
| Authors: | Tomar, Radha Suwasia, Sonam Choudhury, Angshuman Roy Venkataramani, Sugumar Babu, Srinivasarao Arulananda |
| Keywords: | amino acid scaffolds Mills azo coupling arylation strategy |
| Issue Date: | 2022 |
| Publisher: | Royal Society of Chemistry |
| Citation: | Chemical Communications, 58(93), 12967-12970 |
| Abstract: | Azobenzene-based unnatural amino acid motifs were synthesized via Pd(II)-catalyzed diastereoselective C(sp3)–H arylation of amino acid carboxamides with iodoacetanilides and Mills azo coupling. |
| Description: | Only IISERM authors are available in the record. |
| URI: | https://doi.org/10.1039/d2cc04870a http://hdl.handle.net/123456789/4476 |
| Appears in Collections: | Research Articles |
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|---|---|---|---|---|
| Need To Add…Full Text_PDF..pdf | 15.36 kB | Adobe PDF | View/Open |
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