
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/5035
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DC Field | Value | Language |
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dc.contributor.author | Pandey, Rajat | - |
dc.contributor.author | Singh, Gurdeep | - |
dc.contributor.author | Gour, Vinod | - |
dc.contributor.author | Anand, Ramasamy Vijaya | - |
dc.date.accessioned | 2023-08-22T12:03:14Z | - |
dc.date.available | 2023-08-22T12:03:14Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Tetrahedron, 82, 131950. | en_US |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0040402021000417?via%3Dihub | - |
dc.identifier.uri | http://hdl.handle.net/123456789/5035 | - |
dc.description | Only IISER Mohali authors are available in the record. | en_US |
dc.description.abstract | A one-pot approach has been developed for the synthesis of 2,3-disubstituted indoles through a base-mediated N-alkylation of 2-(tosylamino)aryl-substitued para-quinone methides with halomethylaryl ketones followed by intramolecular cyclization and tosyl group elimination sequence. This one-pot protocol provides direct access to a wide range of 2,3-disubstituted indoles in moderate to good yields under mild conditions. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | Indoles | en_US |
dc.subject | Heterocycles | en_US |
dc.title | Base-mediated sequential one-pot approach for the synthesis of 2,3-disubstituted indoles from 2-(tosylamino)aryl-substituted para-quinone methides | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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