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http://hdl.handle.net/123456789/1326Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kumar, Suresh | - |
| dc.date.accessioned | 2019-11-04T10:04:30Z | - |
| dc.date.available | 2019-11-04T10:04:30Z | - |
| dc.date.issued | 2019-11-04 | - |
| dc.identifier.uri | IISERM | en_US |
| dc.identifier.uri | http://hdl.handle.net/123456789/1326 | - |
| dc.description.abstract | Tropylium tetrafluoroboratehas been utilized as a BrØnsted base for the 1,6-conjugate addition of indoles to para-quinone methides. This transformation occurs at mild conditions and is tolerant to a variety of functional groups. This protocol provides an easy and straightforward access to a set of unsymmetrical diarylindolylmethanes in good to excellent yield. | en_US |
| dc.description.sponsorship | IISERM | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | IISERM | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | P-Quinone Methides | en_US |
| dc.subject | Aromatic Ions | en_US |
| dc.subject | Plausible Mechanism | en_US |
| dc.subject | Fourier transform infrared spectroscopy | en_US |
| dc.title | Tropylium Tetrafluoroborate Catalyzed 1,6-Conjugate Addition of Indoles to p-Quinone Methides | en_US |
| dc.type | Thesis | en_US |
| dc.guide | Anand, R.V. | - |
| Appears in Collections: | MS-14 | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| MS14060.pdf | Full Text.pdf | 3.88 MB | Adobe PDF | View/Open |
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