Loading...
Please wait, while we are loading the content...
Efficient Alkylation of Nitrogen Heterocycles Using Lithium Salts and Oxygen Leaving Groups
| Content Provider | Scilit |
|---|---|
| Author | Epling, Gary A. Kumar, Anil |
| Copyright Year | 1991 |
| Description | Superior yields of N-alkylated nitrogen heterocycles have been achieved with remarkable regioselectivity. The lithium salt of the heterocycle was prepared by treatment with butyllithium in tetrahydrofuran. Reaction of this salt at room temperature with electrophiles, such as alkyl methanesulfonates and 1,2-epoxypropane, bearing an oxygen leaving group proceeded quantitatively and gave exclusive N-alkylation with no detectable C-alkylation. |
| Related Links | http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1991-34743.pdf |
| Ending Page | 348 |
| Page Count | 2 |
| Starting Page | 347 |
| ISSN | 09365214 |
| e-ISSN | 14372096 |
| DOI | 10.1055/s-1991-34743 |
| Journal | Synlett |
| Issue Number | 05 |
| Volume Number | 1991 |
| Language | English |
| Publisher | Georg Thieme Verlag KG |
| Publisher Date | 1991-01-01 |
| Access Restriction | Open |
| Subject Keyword | Organic Chemistry Nitrogen Heterocycles |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry |