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http://hdl.handle.net/123456789/4476Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Tomar, Radha | - |
| dc.contributor.author | Suwasia, Sonam | - |
| dc.contributor.author | Choudhury, Angshuman Roy | - |
| dc.contributor.author | Venkataramani, Sugumar | - |
| dc.contributor.author | Babu, Srinivasarao Arulananda | - |
| dc.date.accessioned | 2023-08-10T13:34:16Z | - |
| dc.date.available | 2023-08-10T13:34:16Z | - |
| dc.date.issued | 2022 | - |
| dc.identifier.citation | Chemical Communications, 58(93), 12967-12970 | en_US |
| dc.identifier.uri | https://doi.org/10.1039/d2cc04870a | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/4476 | - |
| dc.description | Only IISERM authors are available in the record. | en_US |
| dc.description.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. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | Royal Society of Chemistry | en_US |
| dc.subject | amino acid scaffolds | en_US |
| dc.subject | Mills azo coupling | en_US |
| dc.subject | arylation strategy | en_US |
| dc.title | Azobenzene-based unnatural amino acid scaffolds via a Pd(II)-catalyzed C(sp3)–H arylation strategy | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Research Articles | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Need To Add…Full Text_PDF..pdf | 15.36 kB | Adobe PDF | View/Open |
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