4-Dihydroxy-3-(indol-2-)-yl-quinoline via substantial methodology-fisher indole synthesis
| dc.contributor.author | Pitchai, P. | en_US |
| dc.contributor.author | Nepolraj, A. | en_US |
| dc.contributor.author | Sathiyaseelan, M. | en_US |
| dc.contributor.author | Gengan, Robert Moonsamy | en_US |
| dc.date.accessioned | 2018-06-04T06:39:37Z | |
| dc.date.available | 2018-06-04T06:39:37Z | |
| dc.date.issued | 2016 | |
| dc.description.abstract | Fisher indole methodology, a simple application was used to generate indole as a substitution on the quinoline ring. Conventional heating and microwave irradiation was compared. The ease of work up procedure, reduced time and moreover the high yield is exceptional however microwave irradiation presented more advantages. | en_US |
| dc.dut-rims.pubnum | DUT-005855 | en_US |
| dc.format.extent | 4 p | en_US |
| dc.identifier.citation | Pitchai, P. et al. 2016. 4-Dihydroxy-3-(indol-2-)-yl-quinoline via substantial methodology-fisher indole synthesis. Heterocyclic Letters. 6(1): 11-14. | en_US |
| dc.identifier.issn | 2231–3087 (print) | |
| dc.identifier.issn | 2230-9632 (online) | |
| dc.identifier.uri | http://hdl.handle.net/10321/3008 | |
| dc.language.iso | en | en_US |
| dc.publisher | Heterocyclic Letters | en_US |
| dc.publisher.uri | http://www.heteroletters.org/issue16/PDF/Paper-1.pdf | en_US |
| dc.relation.ispartof | Heterocyclic letters | en_US |
| dc.subject | Indole | en_US |
| dc.subject | Quinoline | en_US |
| dc.subject | Fisher-indole method | en_US |
| dc.subject | 3-acyl-2 | en_US |
| dc.subject | 4-dihydroxyquinoline | en_US |
| dc.title | 4-Dihydroxy-3-(indol-2-)-yl-quinoline via substantial methodology-fisher indole synthesis | en_US |
| dc.type | Article | en_US |