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A Facile Synthetic Route towards Substituted Thieno[3,2-e]indoles
| Content Provider | Scilit |
|---|---|
| Author | Dehaen, Wim Snick, Wim Van Nulens, Wienand Jambon, Sarah |
| Copyright Year | 2009 |
| Description | A number of substituted thieno[3,2-e]indoles have been prepared in high yields via a tetrabutylammonium fluoride mediated cyclization of 5-acetamido-4-ethynylbenzothiophenes, which, in turn, are easily accessible from the corresponding 4-iodobenzothiophenes. This method presents a viable alternative to the traditionally used Fischer indolization procedures. |
| Related Links | http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0028-1083366.pdf |
| Ending Page | 774 |
| Page Count | 8 |
| Starting Page | 767 |
| ISSN | 00397881 |
| e-ISSN | 1437210X |
| DOI | 10.1055/s-0028-1083366 |
| Journal | Synthesis |
| Issue Number | 05 |
| Volume Number | 2009 |
| Language | English |
| Publisher | Georg Thieme Verlag KG |
| Publisher Date | 2009-02-11 |
| Access Restriction | Open |
| Subject Keyword | Journal: Synthesis Organic Chemistry Fused-ring Systems Tetrabutylammonium Fluoride |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry Catalysis |