Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/1914Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jadhav, A.S. | - |
| dc.contributor.author | Pankhade, Y.A. | - |
| dc.contributor.author | Anand, R.V. | - |
| dc.date.accessioned | 2020-11-19T10:11:16Z | - |
| dc.date.available | 2020-11-19T10:11:16Z | - |
| dc.date.issued | 2018 | - |
| dc.identifier.citation | Journal of Organic Chemistry, 83(15), pp. 8615-8626 | en_US |
| dc.identifier.other | https://doi.org/10.1021/acs.joc.8b00607 | - |
| dc.identifier.uri | https://pubs.acs.org/doi/abs/10.1021/acs.joc.8b00607 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/1914 | - |
| dc.description.abstract | An effective method for the construction of the structurally complex fused cyclohepta[b]indole core has been developed through an intermolecular 1,6-conjugate addition of indoles to 2-alkynyl p-quinone methides followed by an intramolecular electrophilic cyclization under oxophilic and alkynophilic gold catalysis. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.subject | 1 ,6-conjugate additions | en_US |
| dc.subject | Electrophilic cyclization | en_US |
| dc.subject | p-Quinone methides | en_US |
| dc.subject | Cyclization | en_US |
| dc.subject | quinone derivative | en_US |
| dc.subject | electrophilicity | en_US |
| dc.title | Exploring Gold Catalysis in a 1,6-Conjugate Addition/Domino Electrophilic Cyclization Cascade: Synthesis of Cyclohepta[b]indoles | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Research Articles | |
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| File | Description | Size | Format | |
|---|---|---|---|---|
| Need to add pdf.odt | 8.63 kB | OpenDocument Text | View/Open |
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