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N-Arylation of Heterocycles by a Tandem Aza-Michael Addition Reaction and Aromatization Sequence
| Content Provider | Scilit |
|---|---|
| Author | Chittimalla, Santhosh Kumar Nakka, Srinuvasu Koodalingam, Manikandan Bandi, Chennakesavulu |
| Copyright Year | 2017 |
| Description | Cyclohexa-2,4-dien-1-one derivatives, upon reaction with N-heterocycles in the presence of scandium(III) triflate, underwent a tandem Michael addition reaction followed by aromatization of the Michael adduct generated in situ to give N-aryl heterocycles in good yields. Because of the ready accessibility of variously substituted cyclohexa-2,4-dien-1-ones, a range of N-aryl heterocycles have become available. |
| Related Links | http://pdfs.semanticscholar.org/e4f0/767d47d98f06fd292567c0087a8d7b25d5aa.pdf http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1588538.pdf |
| Ending Page | 64 |
| Page Count | 8 |
| Starting Page | 57 |
| ISSN | 09365214 |
| e-ISSN | 14372096 |
| DOI | 10.1055/s-0036-1588538 |
| Journal | Synlett |
| Issue Number | 01 |
| Volume Number | 29 |
| Language | English |
| Publisher | Georg Thieme Verlag KG |
| Publisher Date | 2017-08-17 |
| Access Restriction | Open |
| Subject Keyword | Organic Chemistry Cyclohexadienones Aza-michael Reaction Aryl Heterocycles |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry |