| Item Type: | Article |
|---|---|
| Title: | A general one-pot synthesis of 2H-indazoles using an organophosphorus-silane system |
| Creators Name: | Schoene, J., Bel Abed, H., Schmieder, P., Christmann, M. and Nazaré, M. |
| Abstract: | A simple and direct approach for the regioselective construction of the privileged 2H‐indazole scaffold is described. The developed one‐pot strategy involves phospholene‐mediated N−N bond formation to access 2H‐indazoles. The amount of organophosphorus reagent was minimized by recycling the phospholene oxide with organosilane reductants. Starting from functionalized 2‐nitrobenzaldehydes and primary amines, a mild reductive cyclization, involving the use of commercially available phospholene oxide and silanes, delivered a wide variety of substituted 2H‐indazoles in good to excellent yields. |
| Source: | Chemistry - A European Journal |
| ISSN: | 0947-6539 |
| Publisher: | Wiley-Blackwell |
| Volume: | 24 |
| Number: | 36 |
| Page Range: | 9090-9100 |
| Date: | 26 June 2018 |
| Official Publication: | https://doi.org/10.1002/chem.201800763 |
| PubMed: | View item in PubMed |
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