Cobalt(II)–catalyzed C8H alkoxylation of 1-naphthylamine derivatives with alcohols
-
Add time:09/10/2019 Source:sciencedirect.com
An efficient protocol for cobalt (II)-catalyzed regioselective aryl C8H bond alkoxylation of 1-naphthylamine derivatives with readily available alcohols has been developed, demonstrating an efficient approach to 8-alkoxy-1-naphthylamine derivatives with good functional group tolerance. Note that the picolinamide moiety as a bidentate directing group may play a key role in this regioselective transformation.
We also recommend Trading Suppliers and Manufacturers of 1-(4-BROMOPHENOXY)-2-PROPANONE (cas 18621-22-2). Pls Click Website Link as below: cas 18621-22-2 suppliers
Prev:Toward the discovery of dual HCMV–VZV inhibitors: Synthesis, structure activity relationship analysis, and cytotoxicity studies of long chained 2-uracil-3-yl-N-(4-phenoxyphenyl)acetamides
Next:Regular articleTyr115, Gln165 and Trp209 contribute to the 1,2-epoxy-3-(p-nitrophenoxy)propane-conjugating activity of glutathione S-transferase cGSTM1-11) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Toward the discovery of dual HCMV–VZV inhibitors: Synthesis, structure activity relationship analysis, and cytotoxicity studies of long chained 2-uracil-3-yl-N-(4-phenoxyphenyl)acetamides09/09/2019
- 2,4,6-tris-4-(bromophenoxy)-1,3,5-triazine: a hexagonal host framework assembled with robust Br⋯Br trimer synthons09/08/2019
- Synthesis and evaluation of a novel class Hsp90 inhibitors containing 1-phenylpiperazine scaffold09/07/2019
